Search results for "Enone"

showing 10 items of 320 documents

Synthesis and anti-inflammatory activity of chalcone derivatives

1998

Chalcones and their derivatives were synthesized and evaluated for their anti-inflammatory activity. In vitro, chalcones 2, 4, 8, 10 and 13 inhibited degranulation and 5-lipoxygenase in human neutrophils, whereas 11 behaved as scavenger of superoxide. Only four compounds (4-7) inhibited cyclo-oxygenase-2 activity. The majority of these samples showed anti-inflammatory effects in the mouse air pouch model.

ChalconeNeutrophilsmedicine.drug_classLeukotriene B4Clinical BiochemistryPharmaceutical ScienceLeukotriene B4BiochemistryChemical synthesisAnti-inflammatoryMiceStructure-Activity Relationshipchemistry.chemical_compoundChalconeIn vivoDrug DiscoverymedicineAnimalsHumansCyclooxygenase InhibitorsLipoxygenase InhibitorsMolecular BiologyPropiophenonesArachidonate 5-LipoxygenaseCyclooxygenase 2 InhibitorsMolecular StructureChemistrySuperoxideAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryDegranulationMembrane ProteinsIn vitroIsoenzymesBiochemistryCyclooxygenase 2Prostaglandin-Endoperoxide SynthasesDrug DesignMolecular MedicineBioorganic & Medicinal Chemistry Letters
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E-2-Benzylidenebenzocycloalkanones. IV. Studies on transmission of substituent effects on 13C NMR chemical shifts of E-2-(X-benzylidene)-1-tetralones…

2005

Abstract Single substituent parameter (SSP) and dual substituent parameter (DSP) analyses were applied to study the transmission of substituent effects on selected 13C NMR chemical shifts of the cyclic chalcone analogues, E-2-(4′-X-benzylidene)-1-tetralones (2) and E-2-(4′-X-benzylidene)-1-benzosuberones (3). In order to study how the geometry of the cyclic chalcone analogues affects the transmission of substituent effects similar investigations with the respective chalcones (4) were also performed. The results obtained earlier with the five-membered analogue E-2-(4′-X-benzylidene)-1-indanones (1) were also involved in the comparisons. Geometry optimization of the unsubstituted 1a, 2a, 3a a…

ChalconeStereochemistryChemical shiftOrganic ChemistrySubstituentAb initioCarbon-13 NMRResonance (chemistry)Analytical ChemistryInorganic Chemistrychemistry.chemical_compoundchemistryComputational chemistryEnoneSpectroscopyTetralonesJournal of Molecular Structure
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The reaction of aromatic α,β-unsaturated ketones with 4,5-diamino-1,6- dihydropyrimidin-6-ones

1994

The reaction of 4,5-diamino-1,6-dihydropyrimidin-6-ones 1 with one equivalent of the chalcones 2 leads in an acidic medium to the formation of the 2,4-diaryl-2,3,6,7-tetrahydro-1H-pyrimido[4,5-b][1,4]diazepin-6-ones 3a-m. The structure elucidation of the products is based on detailed nmr investigations including selective 13C[1H] decoupling experiments.

Chalconechemistry.chemical_compoundchemistryBicyclic moleculeDiamineOrganic ChemistryLactamOrganic chemistryEnoneDecoupling (electronics)
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The effect of the fused-ring substituent on anthracene chalcones: crystal structural and DFT studies of 1-(anthracen-9-yl)-3-(naphthalen-2-yl)prop-2-…

2018

Two new anthracene chalcones, namely 1-(anthracen-9-yl)-3-(naphthalen-2-yl)prop-2-en-1-one and 1-(anthracen-9-yl)-3-(pyren-1-yl)prop-2-en-1-one, have been successfully synthesized and the effect of the different fused ring substituent system attached to the anthracene chalcone derivative investigated. These compounds show a very narrow band gap due to the large p-conjugated systems, making them promising candidates as optoelectronic materials. Hirshfeld surface analysis has been carried out to show the contribution of inter­molecular contacts and weak inter­actions to supra­molecular stabilization.

Chalconecrystal structureSubstituentchalconeCrystal structure010402 general chemistry010403 inorganic & nuclear chemistryRing (chemistry)01 natural sciencesMedicinal chemistryDFTResearch Communicationschemistry.chemical_compoundMoietyGeneral Materials ScienceAnthraceneCrystallographyHirshfeld surfaceUV-VisGeneral ChemistryCondensed Matter Physics0104 chemical scienceschemistryQD901-999Density functional theoryEnoneActa crystallographica. Section E, Crystallographic communications
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Rapid hydrolysis of benzodiazepines to benzophenones in a microwave oven

1989

Abstract A microwave oven is used to carry out the complete hydrolysis of diazepam to the corresponding benzophenone in only 10 min, at 650 W, with good recovery. The reaction yield is evaluated by first-derivative UV spectrophotometry.

ChemistryMicrowave ovenBiochemistryAnalytical Chemistrychemistry.chemical_compoundHydrolysisReaction rate constantBenzophenoneEnvironmental ChemistryOrganic chemistrySpectroscopyMicrowaveNuclear chemistryUv spectrophotometryAnalytica Chimica Acta
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Installation of Amine Moieties into a Polycyclic Anodic Product Derived from 2,4-Dimethylphenol

2011

When 2,4-dimethylphenol is anodically treated, a dehydrotetramer with four contiguous stereocentres is readily obtained on a multi-gram scale. The substitution of a 2,4-dimethyl-phenoxy fragment by several amines was demonstrated, and the best results were obtained with primary amines. Optically pure α-chiral aliphatic amines yield diastereomeric mixtures that can be separated in most cases. The basic amine causes a partial hemiketal-opening of the bisbenzofuran moiety leading to an equilibrium within an α,β-unsaturated cyclohexenone. This dynamic behaviour occurs on the time scale of NMR spectroscopy and is also found by X-ray analysis providing a consistent picture.

ChemistryOrganic ChemistryDiastereomerGeneral ChemistryNuclear magnetic resonance spectroscopyCatalysisChiral resolutionchemistry.chemical_compoundCyclohexenoneYield (chemistry)MoietyOrganic chemistryAmine gas treatingAminationChemistry - A European Journal
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Ab initioanalysis on metal ion catalysis in the enolization reactions of some acetylheterocycles: kinetics of the enolization reactions of 3-acetyl-5…

2002

Kinetic data on the enolization reaction of 3-acetyl-5-methylisoxazole, 5-acetyl-3-methylisoxazole, 3(5)-acetylpyrazole and some previously studied acetylheterocycles have been the object of a comprehensive ab initio analysis. Enolization rate constants were measured spectrophotometrically by the halogen trapping technique at 25 °C and ionic strength of 0.3 mol dm−3 in water, in acetate buffers, in dilute hydrochloric acid, in dilute sodium hydroxide and in the presence of some metal ion salts. In the spontaneous (water) and base (acetate) catalysed reactions the ketones investigated are generally more reactive than acetophenone, according to the electron-withdrawing effect of the heterocyc…

ChemistryOrganic ChemistryHeteroatomInorganic chemistryAb initioProtonationKeto–enol tautomerismCatalysischemistry.chemical_compoundReaction rate constantComputational chemistryAb initio quantum chemistry methodsPhysical and Theoretical ChemistryAcetophenoneJournal of Physical Organic Chemistry
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Pauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. Influence of the alkene on the regioselectivity.

2014

Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.

Ciclització (Química)EthyleneHydrocarbons FluorinatedStereochemistryNorbornadieneQuímica organometàl·licaPharmaceutical ScienceAlkynetrifluoromethylalkynesCrystallography X-RayArticlecyclopentenonesAnalytical ChemistryRing formation (Chemistry)cycloadditionslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryNorbornenechemistry.chemical_classificationPauson-Khand reactionTrifluoromethylMolecular StructureAlkenePauson–Khand reactionOrganic ChemistryRegioselectivityStereoisomerismCobaltEthylenesNorbornaneschemistryOrganometallic chemistryChemistry (miscellaneous)AlkynesregioselectivityMolecular MedicineMolecules (Basel, Switzerland)
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Photocatalytic coalescence of functionalized gold nanoparticles.

2009

A novel strategy for the synthesis of chromophore-functionalized AuNPs with a narrow size distribution is reported. It consists of increasing the size of preprepared NPs by means of a fast (second scale) and clean (light and an organic photocatalyst) method. The results agree with thiolate ligand liberation from the NP surface promoted by photogenerated radicals. This lets gold cores come together and finally coalesce.

Coalescence (physics)Materials sciencePyrenesLigandNanoparticleMetal NanoparticlesSurfaces and InterfacesChromophoreCondensed Matter PhysicsPhotochemistryPhotochemical ProcessesCatalysisCatalysisBenzophenonesTransition metalColloidal goldElectrochemistryPhotocatalysisGeneral Materials ScienceGoldSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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Esse.Re (nel) mondo. Arti visive e rinascita dal 1966 a oggi

2022

Nel complesso quadro distopico della pandemia il saggio prende in esame il progetto espositivo e curatoriale .RE, mostra che non si limita a presentare le ricerche di una selezione di artisti tra i più influenti dei nostri tempi ma si focalizza sull’urgente necessità di problematizzare le dicotomie arte/vita, azione/contemplazione, arte/anti-arte, nella prospettiva di una riflessione critica intorno a una raccolta di opere innovative, tanto nel metodo quanto nel contenuto. Vengono esaminate le opere più significative delle ricerche condotte da Alberto Burri, Saint Clair Cemin, Tony Cragg, Zang Hong Mei, Anselm Kiefer, Jeff Koons, Sol LeWitt, Emil Lukas, Mimmo Paladino, Claudio Parmiggiani, …

Contemporary ArtAlberto Burri Saint Clair Cemin Tony Cragg Zang Hong Mei Anselm Kiefer Jeff Koons Sol LeWitt Emil Lukas Mimmo Paladino Claudio Parmiggiani Giuseppe Penone Michelangelo Pistoletto Tania Pistone Andres Serrano Ai Weiwei Gilberto ZorioSettore L-ART/03 - Storia Dell'Arte ContemporaneaAlberto Burri Saint Clair Cemin Tony Cragg Zang Hong Mei Anselm Kiefer Jeff Koons Sol LeWitt Emil Lukas Mimmo Paladino Claudio Parmiggiani Giuseppe Penone Michelangelo Pistoletto Tania Pistone Andres Serrano Ai Weiwei Gilberto Zorio.Arte contemporanea
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