Search results for "copper"

showing 10 items of 3029 documents

ChemInform Abstract: E,Z-Stereodivergent Synthesis of N-Tosyl α,β-Dehydroamino Esters via a Mukaiyama-Michael Addition

2016

The stereodivergent synthesis of N-tosyl α,β-dehydroamino esters via a Mukaiyama–Michael addition is reported. The reaction of silylketene acetals with N-tosylimines derived from β,γ-unsaturated α-keto esters in dichloromethane provided the corresponding (Z)-α,β-dehydroamino esters while the (E)-isomers were obtained when the reaction was carried out in the presence of 10 mol% copper(II) triflate.

chemistry.chemical_compoundTosylchemistryMichael reactionchemistry.chemical_elementGeneral MedicineMedicinal chemistryTrifluoromethanesulfonateCopperDichloromethaneChemInform
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ChemInform Abstract: Highly Enantioselective Copper(I)-Catalyzed Conjugate Addition of Terminal Alkynes to 1,1-Difluoro-1-(phenylsulfonyl)-3-en-2-one…

2014

A highly enantioselective copper-catalyzed conjugate alkynylation of monoactivated enones, namely 1,1-difluoro-1-(phenylsulfonyl)-3-en-2-ones, is described. The reaction products are obtained with good yields and excellent enantioselectivities (from 92 to 99% ee). The β-alkynylated difluoro(phenylsulfonyl) ketones can be converted into the corresponding β-alkynylated difluoro- and trifluoromethyl ketones, esters and amides. This is the first example on the use of 1,1-difluoro-1-(phenylsulfonyl)-3-en-2-ones as substrates in an enantioselective reaction, which have been shown to be new ester/amide surrogates.

chemistry.chemical_compoundTrifluoromethylAlkynylationChemistryAmideEnantioselective synthesischemistry.chemical_elementGeneral MedicineMedicinal chemistryCopperCatalysisConjugateChemInform
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ChemInform Abstract: Aryl Radicals by Copper(II) Oxidation of Hydrazines: A New Method for the Oxidative and Reductive Arylation of Alkenes.

1990

Abstract A new source of aryl radicals interesting from the preparative point of view has been found in the reaction of arylhydrazines and copper(II) sulfate. The process allows selectively both the reductive and oxidative arylation of alkenes.

chemistry.chemical_compoundchemistryArylRadicalchemistry.chemical_elementGeneral MedicineOxidative phosphorylationSulfateCopperCombinatorial chemistryChemInform
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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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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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Aryl radicals by copper(II) oxidation of hydrazines: A new method for the oxidative and reductive arylation of alkenes

1989

Abstract A new source of aryl radicals interesting from the preparative point of view has been found in the reaction of arylhydrazines and copper(II) sulfate. The process allows selectively both the reductive and oxidative arylation of alkenes.

chemistry.chemical_compoundchemistryRadicalArylOrganic ChemistryDrug Discoverychemistry.chemical_elementOrganic chemistryOxidative phosphorylationSulfateBiochemistryMedicinal chemistryCopperTetrahedron Letters
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Cyclam-strapped porphyrins and their iron(III)-copper(II) complexes as models for the resting state of cytochrome c oxidase

1999

International audience; The ESR study of two cyclam-strapped porphyrins in which, on one side, the cyclam is attached with a variable length linker to the porphyrin and, on the other side, a non-coordinating strap protects the iron from any intermolecular interaction, is reported. Variation of the linker length is made possible by the use of either a Michael reaction or a nucleophilic substitution, leading respectively to three or two carbon atom links. It is shown that in the case of the shortest link, the oxidized ironÈcopper complex exhibits a spin interaction. The distance between thetwo metal centers is evaluated to be around 4.5 Å, a value consistent with the one found in the natural …

chemistry.chemical_element010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisMetalchemistry.chemical_compoundCyclam[CHIM] Chemical SciencesMaterials ChemistryNucleophilic substitutionCytochrome c oxidase[CHIM]Chemical Sciencesbiology010405 organic chemistryGeneral ChemistryPorphyrinCopper0104 chemical sciencesCrystallographychemistryvisual_artvisual_art.visual_art_mediumMichael reactionbiology.proteinLinker
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Electrochemical Characterization of Corrosion Products in Leaded Bronze Sculptures Considering Ohmic Drop Effects on Tafel Analysis

2015

[EN] The characterization of corrosion products in leaded bronze based on the voltammetry of immobilized particles methodology is described. Voltammetric data, supported by Fourier transform infra-red spectroscopy, field emission scanning electron microscopy-energy dispersive X-ray microanalysis (FESEM-EDX) and scanning electrochemical microscopy (SECM) allow the identification of copper and lead corrosion materials. The mutual influence of such products is modeled upon considering uncompensated ohmic drops in the Tafel analysis of the rising portion of the respective voltammetric signals for their electrochemical reduction.

chemistry.chemical_element02 engineering and technologyLeaded copper and bronzeengineering.material01 natural sciencesMicroanalysisUncompensated ohmic dropsAnalytical ChemistryCorrosionScanning electrochemical microscopyElectrochemistryBronzeTafel analysisVoltammetryOhmic contactTafel equationVoltammetry of immobilized particles010401 analytical chemistryMetallurgy021001 nanoscience & nanotechnologyCopper0104 chemical scienceschemistryPINTURAengineering0210 nano-technologySECM
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Spectroscopic, Magnetic, and Electrochemical Studies of a Dimeric N-Substituted-Sulfanilamide Copper(II) Complex. X-ray and Molecular Structure of th…

1997

A copper(II) complex of formula Cu(2)(stz)(4) (stz(-) = sulfathiazolato) has been synthesized and characterized by single-crystal X-ray diffraction. The compound crystallizes in the orthorhombic system, space group P2(1)cn with a = 10.595(7) Å, b = 14.274(3) Å, c = 29.65(1) Å, and Z = 4. The structure consists of dinuclear copper(II) units which contain four sulfathiazolato ligands bridging the metal ions through a nonlinear NCN group. The copper atoms are four-coordinated, the chromophore being CuN(4). The Cu.Cu bond distance is 2.671(2) Å. Magnetic susceptibility data in the temperature range 7-300 K show the occurrence of intramolecular antiferromagnetic coupling with 2J = -61.5 cm(-1). …

chemistry.chemical_elementChromophoreCopperMagnetic susceptibilitylaw.inventionInorganic ChemistryBond lengthCrystallographychemistrylawIntramolecular forceMoleculeOrthorhombic crystal systemPhysical and Theoretical ChemistryElectron paramagnetic resonanceInorganic chemistry
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