Search results for "COMPOUND"

showing 10 items of 35174 documents

Phenolic composition and antioxidant activity in freshly squeezed blood and blond orange juices [citrus sinensis (l.) Osbeck].

2007

phenolics compounds ORAC citrusSettore AGR/15 - Scienze E Tecnologie Alimentari
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Degradation of an alkaloid pheromone from the pale-brown chafer, Phyllopertha diversa (Coleoptera: Scarabaeidae), by an insect olfactory cytochrome P…

1999

AbstractThe pale-brown chafer, Phyllopertha diversa, utilizes an unusual alkaloid, 1,3-dimethyl-2,4-(1H,3H)-quinazolinedione, as its sex pheromone. This compound is rapidly degraded in vitro by the antennal protein extracts from this scarab beetle. Demethylation at the N-1 position and hydroxylation of the aromatic ring have been identified as the major catabolic pathways. The enzyme responsible for the pheromone degradation is membrane-bound, requires NAD(P)H for activity and is sensitive to cytochrome P450 inhibitors, such as proadifen and metyrapone. The ability to metabolize this unusual pheromone was not detected in 12 species tested, indicating that the P450 system, specific to male P…

pheromone-degrading enzymemedia_common.quotation_subjectBiophysicsInsectOlfactionscarab beetleBiochemistryMass SpectrometryHydroxylationchemistry.chemical_compoundAlkaloidsCytochrome P-450 Enzyme SystemStructural BiologyMicrosomesBotanyGeneticsAnimalsCytochrome P-450 Enzyme InhibitorsEnzyme InhibitorsSex AttractantsMolecular BiologyChromatography High Pressure LiquidDemethylationmedia_commonbiologyMolecular StructureProadifenCytochrome P450Cell BiologyMetyraponeProadifenColeopteraBiochemistrychemistrySex pheromonebiology.proteinQuinazolinesPheromoneInsect ProteinsChromatography Thin Layerpheromone inactivationolfactionFEBS letters
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P-C Cross-Coupling Onto Enamides: Versatile Synthesis of α-Enamido Phosphane Derivatives

2012

We report herein the Pd-catalyzed P–C cross-coupling reac- tion between enol phosphates and secondary phosphane–bor- ane complexes or phosphane oxides. The reaction was per- formed under mild conditions, owing to Pd activation of the P–H bonds of the phosphane–boranes (or phosphane oxides) and to the powerful enol phosphate coupling reagents. New useful chiral and achiral α - β -alkenylphosphane derivatives bearing an amido group in the α -position to the P center were obtained in yields up to 70 %.

phosphaalkenesStereochemistryboranesOrganic ChemistryphosphanesBoranesPhosphateEnolMedicinal chemistryCoupling (electronics)chemistry.chemical_compoundchemistryenolsReagentcross-couplingPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Guano-related phosphate-rich minerals in European caves

2019

International audience; Guano is a typical deposit found in caves derived from the excretions of bats and in minor cases of birds. These organic deposits decompose and form a series of acid fluids and gases that can interact with the minerals, sediments, and rocks present in the cave. Over sixty phosphates are known and described from caves, but guano decay also often leads to the formation of nitrates and sulfates. In this study twenty-two European caves were investigated for their guano-related secondary minerals. Using various analytical techniques, seventeen phosphates, along with one sulfate (gypsum), were recognized as secondary products of guano decay. Among those minerals, some are …

phosphatesGypsum010504 meteorology & atmospheric sciencesQH301-705.5Settore GEO/04 - Geografia Fisica E GeomorfologiaGeochemistrybat guanocave minerals phosphate bat guanoengineering.material010502 geochemistry & geophysics01 natural sciencessecondary cave mineralsApatitechemistry.chemical_compoundCavesecondary cave minerals phosphates minerogenesis limestone caves bat guanominerogenesisBiology (General)Sulfatelimestone cavephosphate0105 earth and related environmental sciencesEarth-Surface Processescave mineralsQE1-996.5geographygeography.geographical_feature_categoryMineralSettore GEO/07 - Petrologia E PetrografiaGeology15. Life on landPhosphatehumanitiessecondary cave mineralchemistryminerogenesivisual_artlimestone cavesGuanoengineeringvisual_art.visual_art_mediumPyrite[SDU.STU.MI]Sciences of the Universe [physics]/Earth Sciences/Mineralogy
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SrP3N5O: a highly condensed layer phosphate structure solved from a nanocrystal by automated electron diffraction tomography.

2011

The oxonitridophosphate SrP(3)N(5)O has been synthesized by heating a multicomponent reactant mixture that consisted of phosphoryl triamide OP(NH(2))(3), thiophosphoryl triamide SP(NH(2))(3), SrS, and NH(4)Cl enclosed in evacuated and sealed silica-glass ampoules up to 750 °C. The compound was obtained as nanocrystalline powder with needle-shaped crystallites. The crystal structure was solved ab initio on the basis of electron diffraction data by means of automated electron diffraction tomography (ADT) and verified by Rietveld refinement with X-ray powder diffraction data. SrP(3)N(5)O crystallizes in the orthorhombic space group Pnma (no. 62) with unit-cell data of a=18.331(2), b=8.086(1), …

phosphatesRietveld refinementChemistryOrganic ChemistryAb initioGeneral ChemistryCrystal structureelectron diffraction; layered compounds; oxonitrides; phosphates; strontiumoxonitridesCatalysisNMR spectra databaseCrystallographyElectron diffractionlayered compoundselectron diffractionOrthorhombic crystal systemCrystallitestrontiumPowder diffractionChemistry (Weinheim an der Bergstrasse, Germany)
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Designing P-Chirogenic 1,2-Diphosphinobenzenes at Both P-Centers Using P(III)-Phosphinites

2016

International audience; A new enantiodivergent synthesis of P-chirogenic 1,2-diphosphinobenzenes (DP*B) bearing the chirality on one or both phosphorus centers is reported using aryne chemistry. The principle is based on successive reactions of 1,2-dibromobenzene with sec-phosphide boranes, then DABCO to remove the borane, and finally with chlorophosphines or P(III)-chirogenic phosphinites. The efficiency of this synthesis was demonstrated by the stereoselective preparation of (S,S)-1,2-bis(o-anisylphenylphosphino)benzene. A comparison of DIPAMP and homochiral DP*B ligands in asymmetric Rh- or Pd-catalyzed reactions was reported.

phosphine-ligandsDIPAMPketonesStereochemistryBoranesDABCOBorane010402 general chemistry[ CHIM ] Chemical Sciences01 natural sciencesBiochemistryArynecatalyzed asymmetric hydrogenationchemistry.chemical_compoundfunctionalized alkenes[ CHIM.ORGA ] Chemical Sciences/Organic chemistry[CHIM]Chemical SciencesorganocatalysisPhysical and Theoretical Chemistryhydroformylation010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistrycarbon-monoxide0104 chemical scienceshighly enantioselective hydrogenationOrganocatalysisderivativesStereoselectivityChirality (chemistry)phospholane ligands
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Herbicidal activity of phosphonic, phosphinic, and phosphonous acid analogues of phenylglycine and phenylalanine

1995

A series of phosphonic, phosphinic, and phosphonous acid analogues of phenylglycine and phenylalanine was synthesized and tested as herbicides against Lepidium sativum and Cucumis sativus. Aminobenzylphosphonic acids exhibited notable herbicidal activity and thus represent a group of the most active herbicides found among aminophosphonic acids.

phosphonic acidStereochemistryfood and beveragesPhenylalanineBiological activityPlant ScienceLepidium sativumchemistry.chemical_compoundchemistryglyphosateGlyphosateacid analogueOrganic chemistryadamantylAgronomy and Crop Scienceherbicidal activityJournal of Plant Growth Regulation
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Surfactant-Mediated Morphology and Photocatalytic Activity of α‑Ag2WO4 Material

2018

In the present work, the morphology (hexagonal rod-like vs cuboid-like) of an α-Ag2WO4 solid-state material is manipulated by a simple controlled-precipitation method, with and without the presence of the anionic surfactant sodium dodecyl sulfate (SDS), respectively, over short reaction times. Characterization techniques, such as X-ray diffraction analysis, Rietveld refinement analysis, Fourier-transform (FT) infrared spectroscopy, FT Raman spectroscopy, UV–vis spectroscopy, transmission electron microscopy (TEM), high-resolution TEM, selected area electron diffraction, energy-dispersive X-ray spectroscopy, field emission-scanning electron microscopy (FE-SEM), and photoluminescence emission…

photocatalytic activityMaterials scienceAnalytical chemistryInfrared spectroscopy02 engineering and technology010402 general chemistry01 natural sciencesdyeslaw.inventionchemistry.chemical_compoundlawmorphologyPhysical and Theoretical ChemistrySodium dodecyl sulfateSpectroscopyinfrared spectroscopyRietveld refinementenamels021001 nanoscience & nanotechnology0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsGeneral EnergychemistryTransmission electron microscopyelectron diffractionSelected area diffractionElectron microscopeWulff construction0210 nano-technology
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TiO2-based photocatalysts impregnated with metallo-porphyrins employed for degradation of 4-nitrophenol in aqueous solutions: role of metal and macro…

2007

Photodegradation of organic compounds in water solutions by means of economically advantageous and environment-friendly processes is a topic of growing interest. In recent years a great attention has been devoted to TiO2-based photocatalysts for the oxidative degradation of various organic pollutants. In this context, we have prepared new photo-catalytic polycrystalline TiO2 systems impregnated with sensitizers, i.e., copper, iron or manganese porphyrins, and investigated their photoactivity for 4-nitrophenol oxidation compared with that of bare TiO2. A significant improvement of the photoreactivity was observed in the case of TiO2 impregnated with copper porphyrin, while only a slight bene…

photochemistryAqueous solutiontitanium dioxideInorganic chemistrychemistry.chemical_elementContext (language use)General ChemistryManganeseporphyrinsPhotochemistryCopperPorphyrinchemistry.chemical_compoundchemistrysensitizersTitanium dioxidePhotocatalysisPhotodegradationphotocatalysisMetallo-porphyrins TiO2 4-nitrophenolResearch on Chemical Intermediates
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Room-Temperature Autoconversion of Free-Base Corrole into Free-Base Porphyrin

2006

International audience

photochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryoxidation010405 organic chemistryFree baseporphyrinoidsGeneral ChemistryGeneral MedicinePhotochemistry010402 general chemistryPorphyrin01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistrycorrole[ CHIM.ORGA ] Chemical Sciences/Organic chemistrynitrogen heterocyclesCorroleComputingMilieux_MISCELLANEOUSAngewandte Chemie
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