Search results for "Molecular Structure"

showing 10 items of 1246 documents

Cu2+ Coordination Properties of a 2-Pyridine Heptaamine Tripod: Characterization and Binding Mechanism

2009

The synthesis, protonation, and Cu(2+) coordination chemistry of a tripodal heptaamine ligand (L(1)) functionalized with 2-pyridine fragments at the ends of its three branches are reported. L(1) presents six relatively high protonation constants followed by much more reduced constant that as indicated by the UV-vis and NMR data, occur on the pyridine fragments. p[H]-metric, ESI/MS(+), EPR and UV-vis data show that L(1) is able to form mono-, di-, and trinuclear Cu(2+) complexes. Slippage movements and molecular reorganizations have been observed to occur as a function of p[H] in the 1:1 Cu(2+) complexes. The kinetic studies showed that the complex formation is fast and proceeds through a di…

chemistry.chemical_classificationSpectrometry Mass Electrospray IonizationMolecular StructurePyridinesStereochemistryTripod (photography)ProtonationHydrogen-Ion ConcentrationLigandsKinetic energyAcid excesslaw.inventionCoordination complexInorganic Chemistrychemistry.chemical_compoundCrystallographyReaction rate constantchemistrylawPyridinePolyaminesProtonsPhysical and Theoretical ChemistryElectron paramagnetic resonanceCopperInorganic Chemistry
researchProduct

d-Glucose as a multivalent chiral scaffold for combinatorial chemistry

2002

Due to their high density of functional groups and their availability in a variety of diastereomeric forms, monosaccharides are considered attractive scaffolds for combinatorial chemistry that allow the attachment and defined spatial alignment of up to five different pharmacophoric groups. For their application in combinatorial syntheses on solid phase, a set of selectively removable hydroxy protecting groups in combination with a cleavable anchor is required. Herein, we report on the construction and use of a versatile multivalent glucose building block for parallel synthesis on the solid phase.

chemistry.chemical_classificationSpectrometry Mass Electrospray IonizationScaffoldAlkylationMolecular StructureStereochemistryOrganic ChemistryDiastereomerHigh densityGeneral MedicineCrystallography X-RayBiochemistryCombinatorial chemistryAnalytical Chemistrychemistry.chemical_compoundCross-Linking ReagentsGlucosechemistryThioglycosidesD-GlucoseCombinatorial Chemistry TechniquesMonosaccharideChromatography High Pressure LiquidCarbohydrate Research
researchProduct

A new dibenzofuran and other constituents from Ligularia caloxantha, a Chinese medicinal plant.

2008

A new dibenzofuran named 1,2,4-trimethyl-7,8-dimethoxy-dibenzofuran (1), together with seven known compounds, euparin (2), 2,5-diacetyl-6-hydroxy-benzofuran (3), 2-acetyl-5,6-dimethoxy-benzofuran (4), gummosogenin (5), lupeol (6), stigmasterol (7) and (E)-2,5-dihydroxy-cinnamic acid (8), were isolated from the roots of Ligularia caloxantha, a Chinese medicinal plant. The structures of the compounds were elucidated by spectroscopic methods.

chemistry.chemical_classificationStigmasterolMolecular StructureChemistryOrganic ChemistryPlant ScienceLigularia caloxanthaAsteraceaeBiochemistryPlant RootsAnalytical ChemistryDibenzofuranchemistry.chemical_compoundTriterpeneOrganic chemistryBenzofuranLupeolBenzofuransDrugs Chinese HerbalNatural product research
researchProduct

Heterogeneous oxidation of pyrimidine and alkyl thioethers in ionic liquids over mesoporous Ti or Ti/Ge catalysts.

2004

Heterogeneous catalytic oxidation of a series of thioethers (2-thiomethylpyrimidine, 2-thiomethyl-4,6-dimethyl-pyrimidine, 2-thiobenzylpyrimidine, 2-thiobenzyl-4,6-dimethylpyrimidine, thioanisole, and n-heptyl methyl sulfide) was performed in ionic liquids by using MCM-41 and UVM-type mesoporous catalysts containing Ti, or Ti and Ge. A range of triflate, tetrafluoroborate, trifluoroacetate, lactate and bis(trifluoromethanesulfonyl)-imide-based ionic liquids were used. The oxidations were carried out by using anhydrous hydrogen peroxide or the urea-hydrogen peroxide adduct and showed that ionic liquids are very effective solvents, achieving greater reactivity and selectivity than reactions p…

chemistry.chemical_classificationTitaniumMolecular StructureChemistryGermaniumOrganic ChemistryThioanisoleInorganic chemistryGeneral ChemistrySulfidesHeterogeneous catalysisSilicon DioxidePeroxideCatalysisCatalysischemistry.chemical_compoundPyrimidinesCatalytic oxidationIonic liquidSolventsParticle SizeTrifluoromethanesulfonateOxidation-ReductionPorosityAlkylChemistry (Weinheim an der Bergstrasse, Germany)
researchProduct

Fluorous (Trimethylsilyl)ethanol:  A New Reagent for Carboxylic Acid Tagging and Protection in Peptide Synthesis

2006

Starting with a fluorous analogue of 2-(trimethylsilyl)ethanol, we have designed an easy method for preparing a new fluorous tag ((F)TMSE) for the protection of carboxylic acids. Because mild conditions are employed in the tag cleavage (TBAF in the presence of 4 A molecular sieves, which prevent racemization), this tag can be advantageously used in the synthesis of peptides and modified peptides, as we have demonstrated with several examples, including the fluorous synthesis of short alpha- and beta-peptides as well as of modified fluorinated retropeptides.

chemistry.chemical_classificationTrimethylsilyl CompoundsEthanolMolecular StructureTrimethylsilylChemistryCarboxylic acidOrganic ChemistryCarboxylic AcidsPeptideChemical synthesischemistry.chemical_compoundReagentPeptide synthesisOrganic chemistryPeptidesRacemizationThe Journal of Organic Chemistry
researchProduct

Acetylcholine esterase: the structure.

1991

chemistry.chemical_classificationbiologyMolecular StructureSpatial structureProtein ConformationActive siteBiochemistryAcetylcholinesteraseAcetylcholine esterasechemistry.chemical_compoundEnzymeProtein structurechemistryBiochemistrybiology.proteinAcetylcholinesteraseMolecular BiologyTrends in biochemical sciences
researchProduct

Rhodium catalyzed oxidative coupling of salicylaldehydes with diazabicyclic olefins: a one pot strategy involving aldehyde C–H cleavage and π-allyl c…

2013

An efficient one pot strategy for the synthesis of cyclopentene fused chromanone derivatives through the direct oxidative coupling of salicylaldehydes with bicyclic olefins in the presence of a rhodium-copper catalyst system is described. This is the first report on the ring opening-ring closing of bicyclic hydrazines via metal catalyzed oxidative coupling reaction.

chemistry.chemical_elementAlkenesRing (chemistry)Medicinal chemistryAldehydeCatalysisCatalysisRhodiumchemistry.chemical_compoundMaterials ChemistryOrganic chemistryMoleculeCyclopenteneRhodiumta116chemistry.chemical_classificationAldehydesAza CompoundsMolecular StructureOxidative CouplingBicyclic moleculeMetals and AlloysGeneral ChemistrySurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialschemistryChromonesCyclizationCeramics and CompositesOxidative coupling of methaneChemical Communications
researchProduct

Modular Approach to 9-Monosubstituted Fluorene Derivatives Using Mo(V) Reagents.

2016

Oxidative coupling using molybdenum(V) reagents provides fast access to highly functionalized 9-monosubstituted fluorenes. This synthetic approach is highly modular, is high yielding, and tolerates a variety of labile moieties, e.g. amides or iodo groups. The established protocol leads to promising precursors for pharmacologically important analogues of melatonin.

chemistry.chemical_elementFluorene010402 general chemistry01 natural sciencesBiochemistryHigh yieldingchemistry.chemical_compoundMoleculeOrganic chemistryCombinatorial Chemistry TechniquesPhysical and Theoretical ChemistryMelatoninMolybdenumFluorenesMolecular StructureOxidative Coupling010405 organic chemistrybusiness.industryOrganic ChemistryModular design0104 chemical scienceschemistryMolybdenumReagentOxidative coupling of methaneIndicators and ReagentsbusinessOrganic letters
researchProduct

Palladium-based catalytic systems for the synthesis of conjugated enynes by Sonogashira reactions and related alkynylations

2007

Conjugated alkynes are recurring building blocks in natural products, a wide range of industrial intermediates, pharmaceuticals and agrochemicals, and molecular materials for optics and electronics. The palladium-catalyzed cross-coupling between sp(2)-hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with sp-hybridized carbon atoms of terminal acetylenes is one of the most important developments in the field of alkyne chemistry over the past 50 years. The seminal work of the 1970s has initiated an intense search for more general and reliable reaction conditions. The interest in the catalytic activation of demanding substrates, the need to minimize the consumption of depletive r…

chemistry.chemical_elementSonogashira couplingAlkyneHalideConjugated systemHeterogeneous catalysis010402 general chemistryalkynes01 natural sciencesCatalysisCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/CatalysisOrganometallic Compoundscross-couplingOrganic chemistryComputingMilieux_MISCELLANEOUSchemistry.chemical_classificationMolecular Structure010405 organic chemistryArylStereoisomerismGeneral ChemistryGeneral Medicine[CHIM.CATA]Chemical Sciences/Catalysissonogashira reactionspalladiumCombinatorial chemistry0104 chemical sciencesheterogeneous catalysischemistryCarbonPalladium
researchProduct

An Overview on the Performance of 1,2,3-Triazole Derivatives as Corrosion Inhibitors for Metal Surfaces

2021

This review accounts for the most recent and significant research results from the literature on the design and synthesis of 1,2,3-triazole compounds and their usefulness as molecular well-defined corrosion inhibitors for steels, copper, iron, aluminum, and their alloys in several aggressive media. Of particular interest are the 1,4-disubstituted 1,2,3-triazole derivatives prepared in a regioselective manner under copper-catalyzed azide-alkyne cycloaddition (CuAAC) click reactions. They are easily and straightforwardly prepared compounds, non-toxic, environmentally friendly, and stable products to the hydrolysis under acidic conditions. Moreover, they have shown a good efficiency as corrosi…

corrosion inhibitorAzidesmetalQH301-705.5Surface PropertiesReviewCatalysisInorganic ChemistryPhysical and Theoretical ChemistryBiology (General)metal alloysMolecular BiologyQD1-999Spectroscopymechanism of inhibitionCycloaddition ReactionMolecular StructureOrganic ChemistryGeneral MedicineQuímicaTriazolesComputer Science ApplicationsCorrosionChemistryMetalsclick chemistry123-triazoleInternational Journal of Molecular Sciences
researchProduct