Search results for "nuclear magnetic resonance"

showing 10 items of 1743 documents

Predominance of resonance over polar effects on1H,13C and15N NMR substituent chemical shifts inN-arylglycines

1998

chemistry.chemical_compoundNuclear magnetic resonancechemistryChemical shiftSubstituentProton NMRResonancePolarGeneral Materials ScienceGeneral ChemistryCarbon-13 NMRMagnetic Resonance in Chemistry
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13C nuclear magnetic resonance spectra of several podocarpane and cassane diterpenoids

1990

The 13C NMR spectra of several diterpenic derivatives having the podocarpane and cassane skeleton were recorded and interpreted. The most significant effects due to substituent orientation, B/C ring junction stereochemistry and conformational changes are briefly discussed.

chemistry.chemical_compoundNuclear magnetic resonancechemistryStereochemistrySubstituentChemical solutionGeneral Materials ScienceGeneral ChemistryNuclear magnetic resonance spectroscopyCarbon-13 NMRDiterpeneSpectral lineMagnetic Resonance in Chemistry
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Antidiabetische wirkstoffe. V Lang- und verzweigtkettig substituierte chlor-dihexylamino-1,3,5-triazine

1985

Die nucleophile Substitution eines Chloratoms in 2,4-Dichlor-6-dihexylamino-1,3,5-triazin (1) durch Amine (2a-c) fuhrt zu den Alkylamino-chlor-dihexylamino-1,3,5-triazinen 3a-c. Fur Strukturtyp 3 typische Signale in den 1H-NMR-Spektren sind das Triplett bei 0,9 ppm fur die endstandigen Methylgruppen und das Multiplett bei 3,3-3,65 ppm fur die den Stickstoffatomen benachbarten Methylengruppen. In Verbindungsklasse 3 finden sich Vertreter mit antidiabetischer, trichomonazider, antiviraler und anthelminthischer Wirksamkeit. The nucleophilic substitution of one chlorine atom in 2,4-dichloro-6-dihexylamino-1,3,5-triazine (1) by amines 2a-c leads to the alkylamino-chlorodihexylamino-1,3,5-triazin…

chemistry.chemical_compoundNucleophilechemistryHexylamineStereochemistryOrganic ChemistryNucleophilic substitutionAmine gas treatingStructure typeDipropylamineNuclear magnetic resonance spectroscopyMethyleneJournal of Heterocyclic Chemistry
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New Sesquiterpene Lactones and Other Constituents fromCentaurea paui

1997

Aerial parts of Centaurea paui afforded, in addition to several known sesquiterpene lactones, the two new elemanolides 2–4, the new elemane derivative 5 as well as the five new heliangolides 14–18. Their structures were elucidated by spectroscopic methods, especially high-field NMR spectroscopy. The structure of the heliangolide 12 previously isolated from this plant, has been confirmed by X-ray diffraction.

chemistry.chemical_compoundPhytochemistryChemistryStereochemistryCentaurea pauiOrganic ChemistryOrganic chemistryGeneral ChemistryNuclear magnetic resonance spectroscopyPhysical and Theoretical ChemistrySesquiterpeneDerivative (chemistry)TerpenoidLiebigs Annalen
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Trichomonazide Wirkstoffe, 2. Mitt. Verzweigtkettig 4,6-disubstituierte 2-Cyanaminopyrimidine

1985

Aus der Umsetzung von Dicyandiamid (1) mit den β-Diketonen 2a–b gehen die 4,6-verzweigtkettig disubstituierten 2-Cyanaminopyrimidine 3a–b hervor. Fur Strukturtyp 3 last sich aus den spektroskopischen Daten, speziell aus den 1H- und 13C-NMR-Werten, das Vorliegen eines Gleichgewichts zwischen den tautomeren 2-Cyanamino- und 2-Cyaniminopyrimidinformen ableiten. 3 zeichnet sich durch trichomonazide, antivirale und antimykotische Wirkung aus. Trichomonacidal Agents, II: 4,6-Disubstituted 2-(Cyanoamino)pyrimidines Carrying Branched Substituents The reaction of dicyandiamide (1) with the β-diketones 2a–b yields the 4,6-branched disubstituted 2-(cyanoamino)pyrimidines 3a–b. From spectroscopic evide…

chemistry.chemical_compoundPyrimidineChemistryStereochemistryDrug DiscoveryPharmaceutical ScienceNuclear magnetic resonance spectroscopyCondensation reactionTautomerArchiv der Pharmazie
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Synthesis of chemisorbed imidazolium and phosphonium cations by reaction of ionic liquid precursors with silica.

2010

The reaction of four different basic ionic liquid precursors with Aerosil®300 is presented. Chemisorbed imidazolium and phosphonium cations, with silanolate anions as part of the silicatic support, were obtained and investigated with various solid state NMR techniques.

chemistry.chemical_compoundSolid-state nuclear magnetic resonancechemistryInorganic chemistryIonic liquidMaterials ChemistryMetals and AlloysCeramics and CompositesGeneral ChemistryPhosphoniumCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChemical communications (Cambridge, England)
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Stereocontrolledα-Alkylation of Fully ProtectedL-Serine

2004

Diastereoselective alkylation of the (2S,4S) and (2R,4S) diastereomers of 3-tert-butyl 4-methyl 2-tert-butyl-1,3-oxazolidine-3,4-dicarboxylate (1a/b) is reported. Formation of both diastereomers of these oxazolidines was achieved by changing the order of protection steps, and their relative and absolute configurations were determined by NOESY spectroscopy. The use of the bulky ring substituent tBu together with Boc as the N-protecting group led to the exclusive formation of only one alkylated diastereomer. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004)

chemistry.chemical_compoundStereochemistryChemistryOrganic ChemistryDiastereomerSubstituentStereoselectivityL serinePhysical and Theoretical ChemistryAlkylationRing (chemistry)Two-dimensional nuclear magnetic resonance spectroscopyEuropean Journal of Organic Chemistry
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Benzodiselenagermoles and spirobisbenzodiselenagermoles

1993

Synthesis of benzodiselenagermoles and bisbenzodiselenagermoles was carried out by transmetallation group 4 group 14 between diselenophenylenezirconocenes and dialkyl-, diaryl- or alkylaryldichlorogermanes, aryltrichlorogermane or germanium tetrachloride. The new compounds were studied by 1H, 77Se NMR and mass spectrometry. In the case of compounds with substituted phenyl groups, double irradiation and 2D NMR experiments were performed to determine the chemical shifts of the two selenium atoms. The crystal structure of a spirobisbenzodiselenagermole has been established by X-ray diffraction analysis.

chemistry.chemical_compoundTransmetalationCrystallographychemistryGroup (periodic table)Chemical shiftchemistry.chemical_elementGeneral ChemistryCrystal structureGermanium tetrachlorideMass spectrometryTwo-dimensional nuclear magnetic resonance spectroscopySeleniumHeteroatom Chemistry
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Multinuclear magnetic resonance study of 1,3,3-trimethylbicyclo [2.2.1]heptan-2-one (fenchone) oxime, its five monochloro derivatives and a dehydroch…

1991

Fenchone oxime, 5-exo-chlorofenchone oxime, 6-exo-chlorofenchone oxime, 7-anti-chlorofenchone oxime, 8-chlorofenchone oxime, 9-chlorofenchone oxime and a dehydrochlorination product of 10-chlorofenchone oxime were synthesized from fenchone and the corresponding chlorofenchones. The 1H, 13C and 17O NMR spectra of the oximes and the dehydrochlorination product were recorded. The NMR data were compared with the corresponding parameters obtained earlier for fenchone and monochlorofenchones in order to determine the differences between the carbonyl and oxime substituents from the NMR spectroscopic point of view, and to assign the stereochemistry of the oxime group. This stereochemistry could not…

chemistry.chemical_compoundchemistryBicyclic moleculeMagnetic resonance studyOrganic chemistryMoleculeGeneral Materials ScienceGeneral ChemistryNuclear magnetic resonance spectroscopyOximeNmr dataFenchoneMagnetic Resonance in Chemistry
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NMR-Spektroskopie an Heterocyclen, 5. Mitt.13C-NMR- und massenspektrometrische Untersuchung N-substituierter Methoxy- und Hydroxy-äthylimidazole

1978

Es wird die 13C-NMR- und massenspektrometrische Untersuchung verschiedener N-substituierter Methoxy- und Hydroxy-athylimidazole beschrieben. Fur den Zerfall von 1,2-Diathyl-4-(2-hydroxyathyl)-imidazol wird ein ausfuhrliches Fragmentierungsschema angegeben. NMR-Spectroscopy of Heterocyclic Compounds, V: 13C-NMR and Mass Spectrometry of N-Substituted (2-Methoxyethyl)- and (2-Hydroxyethyl)-imidazoles The 13C-NMR and mass spectra of various N-substituted (2-methoxyethyl)- and (2-hydroxyethyl)imidazoles are described. A scheme for the fragmentation of 1,2-diethyl-4-(2-hydroxyethyl)imidazole is reported.

chemistry.chemical_compoundchemistryFragmentation (mass spectrometry)Drug DiscoveryMass spectrumPharmaceutical ScienceImidazoleNuclear magnetic resonance spectroscopyMass spectrometryMedicinal chemistryArchiv der Pharmazie
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