Search results for "Nuclear magnetic resonance spectroscopy"

showing 10 items of 843 documents

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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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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Indoloquinolines, Indolobenzoxazines and Quinazolophthalazines Prepared from Norbornane/eneamino Acids and Hydrazides

2005

The reactions of di-endo- and di-exo-aminonorbornane/enecarboxylic acids 1–4 with ethyl 2-(2-oxocyclohexyl)acetate afforded methanoindoloquinolines 5, 6, 8, and 9, the oxo ester participating as a two-membered sp2 building block. In the cases of di-exo- and di-endo-aminonorbornenecarboxylic acids 2 and 4, methanoindolobenzoxazinediones 7 and 10 were also formed; compound 7 was also isolated from the mother liquor of 10. The reactions of ethyl 2-(2-oxocyclohexyl)acetate with aminonorbornane/enecarbohydrazides 11–14 result in the methanoquinazolophthalazines 15–18. The structures of the compounds were elucidated by NMR spectroscopy, and for 6, 7, 8, and 10 also by X-ray crystallography. (© Wi…

chemistry.chemical_compoundchemistryOrganic ChemistryX-ray crystallographyOrganic chemistryNuclear magnetic resonance spectroscopyMother liquorPhysical and Theoretical ChemistryNorbornaneBlock (periodic table)Medicinal chemistryEuropean Journal of Organic Chemistry
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Kronenether mit einem Lewis-sauren Zentrum, eine neue Klasse heterotoper Wirtmoleküle

1991

chemistry.chemical_compoundchemistryStereochemistryGeneral MedicineNuclear magnetic resonance spectroscopyLewis acids and basesCyclophaneAngewandte Chemie
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Aminosäureester als chirale Hilfsgruppen in Lewis-Säure-katalysierten Umsetzungen elektronenreicher Siloxydiene mit Iminen

1990

chemistry.chemical_compoundchemistryStereochemistryImineLactamDiastereomerGeneral MedicineNuclear magnetic resonance spectroscopyCrystal structureLewis acids and basesChirality (chemistry)CatalysisAngewandte Chemie
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Four new eremophilendiolides from Ligularia atroviolacea

2007

From Ligularia atroviolacea, four new eremophilendiolides, 8 beta-hydroxy-eremophil-3,7 (11)-dien-12,8 alpha(14,6 alpha)-diolide (1), 8 beta-methoxy-eremophil-3,7(11)-dien-12,8 alpha(14,6 alpha)-diolide (2), 8 alpha-hydroxy-eremophil-3,7(11)-dien-12,8 beta(14,6 alpha)-diolide (3) and eremophil-3,7(11),8-trien-12,8 (14,6 alpha)-diolide (4), as well as a known diolide (5) were isolated. Their structures were elucidated on the basis of 1D and 2D NMR as well as ESI-MS spectral data. (c) 2006 Yu Zhao. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.

chemistry.chemical_compoundchemistryStereochemistryLigularia atroviolaceaAlpha (ethology)General ChemistrySpectral dataSesquiterpeneBeta (finance)Two-dimensional nuclear magnetic resonance spectroscopyChemical societyChinese Chemical Letters
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