Search results for "AROMA"

showing 10 items of 1006 documents

Preparation and evaluation of lauryl methacrylate monoliths with embedded silver nanoparticles for capillary electrochromatography

2012

In this article, capillary columns constituted by lauryl methacrylate monoliths with embedded silver nanoparticles (AgNPs) were developed and tested. Two incorporation approaches of AgNPs in monoliths were explored. The AgNPs were either photogenerated in situ during polymerization of the monolith by UV irradiation, or incorporated to the polymerization mixture (ex situ). The influence of the AgNP concentration on the morphological and chromatographic properties of the polymer matrix was investigated, and both the in situ and ex situ approaches were comparatively discussed. The morphology of the monoliths was characterized by electron microscopic techniques, and their electrochromatographic…

In situSilverUltraviolet RaysCapillary actionClinical BiochemistryMetal NanoparticlesTocopherolsBiochemistrySilver nanoparticleAnalytical ChemistryMatrix (chemical analysis)Capillary ElectrochromatographyPolycyclic Aromatic HydrocarbonsMonolithchemistry.chemical_classificationCapillary electrochromatographygeographygeography.geographical_feature_categoryChromatographyChemistryFatty AcidsReproducibility of ResultsEstersEquipment DesignPolymerSterolsPolymerizationChemical engineeringMicroscopy Electron ScanningMethacrylatesELECTROPHORESIS
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Synthesis of Fluorinated Indazoles Through ANRORC-Like Rearrangement of 1,2,4-Oxadiazoles with Hydrazine.

2006

A series of 6-substituted fluorinated indazoles has been obtained through an ANRORC-like rearrangement (Addition of Nucleophile, Ring-Opening and Ring-Closure) of 5-tetrafluorophenyl-1,2,4-oxadiazoles with hydrazine. The initial addition of the bidentate nucleophile to the electrophilic C(5) of the 1,2,4-oxadiazole ring, followed by ring opening and ring closure, leads to the formation of fluorinated indazoles in high yield under mild experimental conditions. Functionalization of the C(6) in the final indazole nucleus was preliminarily achieved through a nucleophilic aromatic substitution on the starting 5-pentafluorophenyl-1,2,4-oxadiazole.

IndazoleDenticityOrganic ChemistryHydrazine124-oxadiazoleGeneral MedicineRing (chemistry)BiochemistryMedicinal chemistrychemistry.chemical_compoundchemistryNucleophileNucleophilic aromatic substitutionYield (chemistry)Drug DiscoveryElectrophileindazoleOrganic chemistryfluorinated heterocycleANRORC-like rearrangementsChemInform
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3-Benzyl-3-hy-droxy-2-phenyl-3H-indole 1-oxide.

2010

The asymmetric unit of the title compound, C21H17NO2, contains two crystallographically independent molecules of similar geometry. The indole ring systems form dihedral angles of 8.30 (5) and 9.58 (5)° with the attached phenyl rings, and 56.96 (5) and 57.68 (5)° with the aromatic rings of the respective benzyl groups. The molecular conformations are stabilized by intramolecular C—H...O hydrogen bonds. In the crystal structure, centrosymmetrically related pairs of molecules are linked into dimers through pairs of intermolecular O—H...O hydrogen bonds, generating 12-membered rings with R22(12) motifs. The dimers are…

Indole testChemistryHydrogen bondOxideAromaticityGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)BioinformaticsOrganic Paperslcsh:ChemistryCrystallographychemistry.chemical_compoundlcsh:QD1-999General Materials ScienceActa crystallographica. Section E, Structure reports online
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Two-Step Route to Indoles and Analogues from Haloarenes: A Variation on the Fischer Indole Synthesis

2012

In a new variation on the Fischer indole synthesis, readily available haloarenes are converted into a wide range of indoles in just two steps by halogen-magnesium exchange and quenching with di-tert-butyl azodicarboxylate, followed by reaction with aldehydes or ketones under acidic conditions. The protocol, which is readily extended to the preparation of indole isosteres, 4- and 6-azaindoles and thienopyrroles, obviates the need to prepare potentially toxic aryl hydrazines, simultaneously avoiding undesirable anilines such as naphthylamines.

Indole testQuenching (fluorescence)IndolesHalogenationChemistryArylOrganic ChemistryTwo stepFischer synthesiHalogenationGreen Chemistry TechnologyChemistry Techniques SyntheticHydrocarbons AromaticSettore CHIM/08 - Chimica Farmaceuticachemistry.chemical_compoundIndoleFischer indole synthesisOrganic chemistrythienopyrrolesMagnesiumFischer synthesis; Indoles; azaindoles; thienopyrrolesFischer synthesisazaindolesazaindole
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Polycondensed nitrogen heterocycles. Part13. Pyrrolo[3,2-b]indole by intramolecular nucleophilic substitution reaction in the pyrrole series

1984

An intramolecular nucleophilic substitution in the pyrrole series has been generalized. The behaviour of nitro, chlorine, bromine and iodine as leaving groups towards the nucleophilic amino group was observed. An acid catalyzed mechanism has been proposed.

Indole testSubstitution reactionStereochemistryOrganic ChemistryMedicinal chemistrychemistry.chemical_compoundNucleophilechemistryNucleophilic aromatic substitutionIntramolecular forcepolycyclic compoundsNucleophilic substitutionAcid hydrolysisPyrroleJournal of Heterocyclic Chemistry
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Mechanism of triplet photosensitized Diels-Alder Reaction between indoles and cyclohexadienes: theoretical support for an adiabatic pathway.

2006

Diels-Alder reactions between indoles (InHs) and 1,3-cyclohexadienes (CHDs) were achieved by using aromatic ketones as photosensitizers. For instance, irradiation of deaerated dichloromethane solutions containing benzoylthiophene (BT, 1 mM), indole (20 mM), and phellandrene (40 mM), in the presence of an acylating agent, led to the N-acetylated Diels-Alder cycloadduct in 46% yield (endo:exo ratio of 1.8:1). Energy transfer from the BT triplet to the CHD gave rise to diene dimers as byproducts. Several combinations of CHDs, InHs, and aromatic ketones were tested; the Diels-Alder reaction was found to be a general process, except when the indole nucleus was substituted at position 2 or 7 and …

Indole testchemistry.chemical_classificationchemistry.chemical_compoundReaction mechanismKetoneDienechemistryOrganic ChemistryCyclohexadienesAromatizationTriplet statePhotochemistryDiels–Alder reactionThe Journal of organic chemistry
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Synthesis of Functionalized Indoles with a Trifluoromethy-Substituted Stereogenic Tertiary Carbon Atom Through an Enantioselective Friedel-Crafts Alk…

2010

[EN] Chiral complexes of BINOL-based ligands with zirconium tert-butoxide catalyze the Friedel-Crafts alkylation reaction of indoles with beta-trifluoromethyl-alpha,beta-unsaturated ketones to give functionalized indoles with an asymmetric tertiary carbon center attached to a trifluoromethyl group. The reaction can be applied to a large number of substituted alpha-trifluoromethyl enones and substituted indoles. The expected products were obtained with good yields and ees of up to 99%.

IndolesHydrocarbons FluorinatedAlkylationEnonesStereoisomerismAlkylationElectrophilic aromatic substitutionLigandsMedicinal chemistryCatalysisCatalysisStereocenterchemistry.chemical_compoundAsymmetric catalysisOrganic chemistryCombinatorial Chemistry TechniquesAromatic substitutionFriedel–Crafts reactionTrifluoromethylMolecular StructureChemistryOrganic ChemistryEnantioselective synthesisStereoisomerismGeneral ChemistryKetonesCarbonFISICA APLICADAZirconiumFluorinated compounds
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Traditional fermented sausage ‘Nem chua’ as a source of yeast biocatalysts efficient for the production of the aroma compound γ-decalactone

2013

International audience; The yeast ecosystem of Nem chua, a Vietnamese traditional fermented sausage naturally rich in medium‐chain‐length lipid‐derived flavouring compounds, was investigated to select biocatalysts able to produce the C10‐fatty acid‐derived aroma compound γ‐decalactone. The total number of yeast was about 5 × 104 to 4 × 105 CFU g−1, and eighty four different species were identified from morphological, physiological and 26S rDNA characteristics, with Candida sake and Candida haemulonii being found in all samples. Six strains able to produce γ‐decalactone from castor oil were selected, of which three Yarrowia lipolytica strains were able to produce between 1 and 2 g L−1 in our…

Industrial and Manufacturing Engineeringchemistry.chemical_compoundmedicineAroma compound[SDV.BBM]Life Sciences [q-bio]/Biochemistry Molecular BiologyFood scienceFermentation in food processingAromaAromachemistry.chemical_classificationbiologyFatty acidYarrowiaLipidFermented sausagesLactonebiology.organism_classificationYeastYeastchemistryBiochemistryCastor oilNem chua/nhamFermentation[SDV.AEN]Life Sciences [q-bio]/Food and NutritionFood Sciencemedicine.drugInternational Journal of Food Science & Technology
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Straightforward One-Pot Synthesis of New 4-Phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one Derivatives: X-ray Single Crystal Structure and Hirshfeld Ana…

2022

A straightforward one-pot route for the synthesis of a new 4-phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one is reported form the direct hydrazinolysis of triketo ester and hydrazine hydrate in ethanol. 4-Phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one was subjected to aza-Michael addition and N-alkylation on reaction with a set of alkylating agents in the presence of K2CO3. Hydrazinolysis of 4-phenyl-1,2,5,6-tetraazafluoranthen-3(2H)-one ester to hydrazide and conversion of hydrazide to thiosemicarbazide were successful. X-Ray single crystals analysis and 1H, 13C NMR were used for unambiguous structure confirmation. The O…H, N…H, C…N and C…C in 2, and the N…H, …

Inorganic ChemistryHirshfeld Analysesaromaattiset yhdisteetkemiallinen synteesipolycyclic aromatic heterocyclesfluoranthenes; polycyclic aromatic heterocycles; <i>aza</i>-Michael addition; <i>N</i>-alkylation; Hirshfeld AnalysesGeneral Chemical EngineeringfluoranthenesGeneral Materials Scienceaza-Michael additionN-alkylationheterosykliset yhdisteetCondensed Matter PhysicsCrystals; Volume 12; Issue 2; Pages: 262
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Untersuchungen zur Konformation und elektronischen Struktur von Cyclooctadieninen

1985

Die mit semiempirischer Quantenmechanik vorhergesagten Konformationen und elektronischen Strukturen der Cyclooctadienine 1 und 2 werden experimentell an Hand von 1H-NMR- und PE-Spektren verifiziert. Dabei wird Bezug genommen auf eine Reihe von anderen, verwandten Cycloalkinen 3–5 und Cycloalkenen 6–11. Wahrend die hohe geometrische Ringspannung entscheidenden Einflus auf 1 und 2 hat, ist eine Homoaromatizitat, die auf sechs nahezu eben angeordneten π-Elektronen-Zentren beruht, nicht signifikant. Investigations on the Conformation and the Electronic Structure of Cyclooctadienynes Conformations and electronic structures of the cyclooctadienynes 1 and 2, predicted by semi-empirical quantum mec…

Inorganic ChemistryHomoaromaticityStereochemistryChemistryChemical solutionUltraviolet radiationRing strainChemische Berichte
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