Search results for "element"

showing 10 items of 13601 documents

ChemInform Abstract: Rhodium(III)-Catalyzed Ring-Opening of Strained Olefins Through C-H Activation of O-Acetyl Ketoximes: An Efficient Synthesis of …

2014

An efficient strategy for the stereoselective synthesis of functionalized cyclopentenes and spiro[2.4]heptenes from strained olefins via C–H activation of aryl ketone O-acetyl ketoximes using [RhCl2Cp∗]2 catalyst is described. The results revealed that a wide range of readily accessible aryl and heteroaryl ketoximes are compatible in this method for the ring opening of bicyclic and spirotricyclic olefins.

chemistry.chemical_compoundchemistryBicyclic moleculeArylchemistry.chemical_elementOrganic chemistryStereoselectivityGeneral MedicineAryl ketoneRing (chemistry)Medicinal chemistryRhodiumCatalysisChemInform
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Polycondensed nitrogen heterocycles. Part24. Pyrrolo[3,4-c]isoquinolinone by thermal rearrangement of a pyrrolylbenzotriazinone

1992

Rearrangement under acidic conditions of the pyrrolylbenzotriazinone 7 afforded the pyrrolylbenzamides 10 and 11. By thermal rearrangement instead, the first fully aromatic derivative of the pyrrolo[3,4-c]isoquinoline ring system 9 was obtained.

chemistry.chemical_compoundchemistryBicyclic moleculeOrganic ChemistryThermalLactamchemistry.chemical_elementThermal reactionIsoquinolineRing (chemistry)Medicinal chemistryNitrogenDerivative (chemistry)Journal of Heterocyclic Chemistry
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Oxidative halogenation of substituted pyrroles with cu(II). Part I. Bromination of some 3-acetylpyrroles

1990

3-Acetylpyrroles are brominated with copper(II) bromide. The reaction afforded almost quantitatively only nuclear monobromination. Evidence for the structures of final compounds was by mass spectrometry, 1 H-nuclear magnetic resonance, ir, and elemental analysis

chemistry.chemical_compoundchemistryBromideElemental analysisOrganic ChemistryPolymer chemistryHalogenationchemistry.chemical_elementOxidative phosphorylationMass spectrometryEnoneCopperJournal of Heterocyclic Chemistry
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Oxidative halogenation of substituted pyrroles with cu(II). Part II. Bromination of some ethyl 3-pyrrolecarboxylates and corresponding acids

1990

Ethyl 3-pyrrolecarboxylates and their corresponding acids are brominated with copper(II) bromide. The reaction afforded at 0°, with high-yield nuclear monobromination.

chemistry.chemical_compoundchemistryBromideOrganic ChemistryHalogenationOrganic chemistrychemistry.chemical_elementOxidative phosphorylationCopperJournal of Heterocyclic Chemistry
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ChemInform Abstract: Preparation and Characterization of Tungsten Chalcogenide Photocatalysts.

2010

Tungsten chalcogenides powders have been prepared by sulfidation of WO3 with gaseous H2S. Different mixed WS2/WO3 systems have been obtained by varying the amount of initial WO3 powder, the time, o...

chemistry.chemical_compoundchemistryChalcogenideInorganic chemistrySulfidationchemistry.chemical_elementGeneral MedicineTungstenCharacterization (materials science)ChemInform
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Rational Design of an Enneanuclear Copper(II) Complex with a Metallacyclophane Core

2004

chemistry.chemical_compoundchemistryCore (graph theory)Polymer chemistryRational designchemistry.chemical_elementGeneral MedicineGeneral ChemistryCopperCombinatorial chemistryCatalysisCyclophaneAngewandte Chemie International Edition
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ChemInform Abstract: Iodine-Induced Stereoselective Carbocyclizations - A New Method for the Synthesis of Cyclohexane and Cyclohexene Derivatives.

1989

chemistry.chemical_compoundchemistryCyclohexaneCyclohexeneOrganic chemistrychemistry.chemical_elementStereoselectivityGeneral MedicineIodineChemInform
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ChemInform Abstract: Synthesis of a Tetraazido-Substituted 2-Tetrazene from 1,5- Cyclooctadiene and Iodine Azide.

2010

In contrast to the addition of iodine azide to cyclooctene (1) or 1,3-cyclooctadiene (5), its reaction with 1,5-cyclooctadiene (12) leads mainly to the surprisingly stable tetraazido-substituted 2-tetrazene 14 The structure of this was established by 15N-NMR studies and an X-ray structural analysis. Treatment of 14 with hydrochloric acid yields the diazido-substituted 9-azabicyclo[3.3.1]nonane 20.

chemistry.chemical_compoundchemistryCycloocteneTetrazene15-Cyclooctadienechemistry.chemical_elementHydrochloric acidGeneral MedicineAzideNonaneIodineMedicinal chemistryChemInform
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Synthesis and spectroscopic characterizations of both 1-ethyl-4,8-dihydro-10-methoxy-3-methyl-8-r1-6-r2-dipyrazolo[3,4-b:4′,3′-f]-[1,5]diazocin-5(1H)…

1995

The non-selective methylation of compounds 3a-d using ethereal diazomethane, allowed the synthesis of isomers 4 and 5 which were useful intermediates for the preparation, by a simple approach, of the title compounds 7 and 9. A complete assignment of the chemical shifts to the carbon atoms of the compounds 7 and 9 was performed by different nmr experiments, such as DEPT and XHDEPT for onebond CH correlations and COLOC experiments for long-range C-H correlations.

chemistry.chemical_compoundchemistryDiazomethaneChemical shiftOrganic Chemistrychemistry.chemical_elementMethylationDEPTMedicinal chemistryCarbonJournal of Heterocyclic Chemistry
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Effect of 99mTc elution in vivo from red cells on red cell volumes measured using autologous 99mTc-labeled red cells: comparison with 51Cr method

2020

The purpose of this work was to compare the measured red-cell volume (RCV) using sodium pertechnetate [RCV-99mTc] compared to the reference technique using sodium radiochromate [RCV-51Cr] and to assess the influence of technetium-99 elution on the RCV-99mTc value. Ten patients had simultaneous measurements of RCV-99mTc and RCV-51Cr. Elution of Tc-99m from red blood cells was 2.9% and led to an average overestimation of RCV-99mTc of 3.7%. The introduction of individual tracer elution rates in the RCV-99mTc calculation corrects this overestimation.

chemistry.chemical_compoundchemistryElutionSodiumRadiochemistrychemistry.chemical_elementGeneral MedicineRed cell volumeSodium pertechnetateAnnales de Biologie Clinique
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