Search results for "Oxime"

showing 10 items of 148 documents

Efficient and stereodivergent electrochemical synthesis of optically pure menthylamines.

2011

chemistry.chemical_compoundchemistry010405 organic chemistryOrganic chemistryGeneral Chemistry010402 general chemistryOximeElectrochemistry01 natural sciencesReductive aminationCatalysis0104 chemical sciencesAngewandte Chemie (International ed. in English)
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ChemInform Abstract: Palladium-Catalyzed Alkoxy- and Aminocarbonylation of α-Halomethyl Oxime Ethers: Synthesis of 1,3-Alkoxyimino Esters and 1,3-Alk…

2015

The three component reactions of α-bromomethyl oxime ethers, carbon monoxide, and alcohols or aromatic amines give imino esters and amides, respectively.

chemistry.chemical_compoundchemistryAlkoxy groupOrganic chemistrychemistry.chemical_elementheterocyclic compoundsGeneral MedicineOximeCarbonylationCatalysisCarbon monoxidePalladiumChemInform
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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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Enantioselective Synthesis of 2-Isoxazolines by a One-Flask Conjugate Addition/Oxime-Transfer Process

2009

Enantioselective isoxazoline synthesis: A combination of 1) a catalytic enantioselective conjugate addition of oximes to alpha,beta-unsaturated aldehydes and 2) an acid-catalyzed intramolecular oxime-transfer reaction lead to the first asymmetric synthesis of 3-unsubstituted 2-isoxazolines (see scheme).

chemistry.chemical_compoundchemistryIntramolecular forceOrganic ChemistryEnantioselective synthesisOrganic chemistryGeneral ChemistryOximeCatalysisCatalysisConjugateChemistry - A European Journal
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ChemInform Abstract: Enantioselective Synthesis of 2-Isoxazolines by a One-Flask Conjugate Addition/Oxime-Transfer Process.

2009

Enantioselective isoxazoline synthesis: A combination of 1) a catalytic enantioselective conjugate addition of oximes to alpha,beta-unsaturated aldehydes and 2) an acid-catalyzed intramolecular oxime-transfer reaction lead to the first asymmetric synthesis of 3-unsubstituted 2-isoxazolines (see scheme).

chemistry.chemical_compoundchemistryIntramolecular forceOrganocatalysisEnantioselective synthesisGeneral MedicineOximeCombinatorial chemistryCatalysisConjugateChemInform
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Structure and magnetic properties of a linear oximato-bridged tetranuclear copper(II) complex

1998

Abstract The tetranuclear copper(II) complex of formula [Cu2(dmg)(Hdmg)(terpy)]2(ClO4)2 (1) (H2dmg = dimethylglyoxime and terpy = 2,2′:6′,2″-terpyridine) has been synthesized and its crystal structure determined by X-ray diffraction methods. It crystallizes in the triclinic system, space group P(−1), with a = 14.382(3), b = 13.728(3), c = 8.979(2) A, α = 96.99(2), β = 111.85(2), γ = 111.22(3)°, V = 1465.0(9) A3, Z = 1, Dc = 1.607 g cm−3, Mr = 1418.0, F(000) = 719, λ(Mo Kα) = 0.71073 A, μ(Mo Kα) = 16.61 cm−1 and T = 298 K. A total of 4891 reflections were measured over the range 2 ≤ θ ≤ 25° and 4393 of them were unique (I > 2.5σ(I) and used in the structural analysis. The structure of 1 may …

chemistry.chemical_elementCrystal structureTriclinic crystal systemMagnetic susceptibilityCopperSquare pyramidal molecular geometryInorganic Chemistrychemistry.chemical_compoundCrystallographyPerchlorateDimethylglyoximechemistryMaterials ChemistryPhysical and Theoretical ChemistryCoordination geometryInorganica Chimica Acta
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Hexanuclear copper(ii) cage with {Cu3O⋯H⋯OCu3} core supported by a dicompartmental oxime ligand with m-xylyl spacer: synthesis, molecular structure a…

2010

A new dicompartmental dioxime ligand (H(2)L) with m-xylyl spacer between the donor sites has been synthesised by Schiff-base condensation of α,α'-diamino-m-xylene and diacetyl monooxime. The ligand reacts with copper(ii) salts giving rise to hexanuclear tricationic copper(II) cage complexes [Cu(II)(6)(μ(3)-O···H···O-μ(3))L(3)(H(2)O)(6)]X(3) (X = BF(4), 1a; X = ClO(4), 1b). The complexes have been characterised by different analytical and spectroscopic techniques and confirmed the hexanuclear structure even in solution. Single crystal X-ray diffraction studies of both the complexes revealed a very similar core structure with three dicompartmental ligands supporting two triangular Cu(3)O core…

crystal structureHydrogen bondLigandExchange interactionHexanuclear copper complexchemistry.chemical_elementCrystallography X-RayLigandsOximeHexanuclear copper complex; oxime; crystal structureoximeCopperInorganic ChemistryMagneticschemistry.chemical_compoundCrystallographychemistryUnpaired electronOximesOrganometallic CompoundsMoleculeSingle crystalCopperDalton Transactions
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Crystal structure of 2-hy­droxy­imino-2-(pyridin-2-yl)-N'-[1-(pyridin-2-yl)ethyl­idene]acetohydrazide

2014

The mol­ecule of the title compound is approximately planar with the planes of the two pyridine rings inclined to one another by 5.51 (7)°. In the crystal, mol­ecules are linked by bifurcated O—H⋯(O,N) hydrogen bonds, forming inversion dimers, which are in turn linked via C—H⋯O and C—H⋯N hydrogen bonds, forming sheets lying parallel to (502).

crystal structureacetohydrazidehy­droxy­iminoStackingpyridylethylideneCrystal structureRing (chemistry)Research CommunicationsCrystalchemistry.chemical_compoundAmideπ–π stacking interactionsPyridineGeneral Materials Scienceta116CrystallographyChemistryHydrogen bondGeneral ChemistryCondensed Matter PhysicsOximehydrogen bondingCrystallographyQD901-999π–π stacking inter­actionshydroxyiminopyridyl­ethyl­ideneActa Crystallographica Section E : Structure Reports Online
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Clinical evaluation of automated capillary refill time estimation in dogs and cats

2019

In this study, we clinically evaluated a pulse oximeter-based device for automated capillary refill time (CRT) estimation in dogs and cats. CRT can reveal conditions like shock or anemia in dogs and cats. However, visual CRT estimation has low repeatability, and the available optical systems for automated estimation are not suitable for pets. We evaluated a custom-made portable CRT measuring device on various measurement sites of 12 dogs and 11 cats with parallel visual CRT estimation on the gum by treating veterinarian. The capillary refill was also recorded by a video camera for reference. The visual and video procedures were moderately correlated with the coefficient of 0.61; visual CRT …

dogsgenetic structurespulse oximetermicrocirculationVideo cameraCapillary refill time01 natural scienceslaw.invention010309 optics03 medical and health sciences0302 clinical medicinelawTime estimationPhotoplethysmogram0103 physical sciencesMedicineCATSmedicine.diagnostic_testPulse (signal processing)business.industrycatsRepeatabilityCapillary refill3. Good health:NATURAL SCIENCES::Physics::Atomic and molecular physics [Research Subject Categories]capillary refill testphotoplethysmographybusinessClinical evaluation030217 neurology & neurosurgeryBiomedical engineering
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Theoretical prediction of the photoinduced chemiluminescence of pesticides

2007

Although it is relatively easy to find chemiluminescent (CL) molecules working on the field of direct liquid phase (especially employing strong oxidants), the molecules found as chemiluminescent are normally very weak CL compounds for developing suitable analytical CL-procedures. Therefore, it is mandatory to develop new strategies to enhance in a simple way the native chemiluminescence of such a compounds, and even to increase the number of compounds to be determined by direct chemiluminescence. Photoinduced chemiluminescence (Ph-CL) results in a simple and easily on-line accessible strategy to solve these disadvantages. In the present paper, molecular connectivity, a topological method wh…

medicine.drug_classCarboxamideSulfuric acidOximeAnalytical Chemistrylaw.inventionchemistry.chemical_compoundPotassium permanganatechemistryComputational chemistrylawmedicineOrganic chemistryMoleculePhotodegradationThiocarbamatesChemiluminescenceTalanta
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