Search results for "compounds"

showing 10 items of 3372 documents

A five-step synthesis of (±)-tylophorine via a nitrile-stabilized ammonium ylide.

2012

The Stevens rearrangement of a nitrile-stabilized ammonium ylide is the key step of a very short and practical synthesis of the phenanthroindolizine alkaloid (±)-tylophorine. The method requires only five linear steps and is devoid of any protecting group manipulations.

chemistry.chemical_classificationNitrileMolecular StructureStereochemistryOrganic ChemistryIndolizinesPhenanthrenesQuaternary Ammonium Compoundschemistry.chemical_compoundAlkaloidschemistryStevens rearrangementYlideNitrilesOrganic chemistryAmmoniumProtecting groupThe Journal of organic chemistry
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Facile access to foldable redox-active flavin-peptide conjugates

2021

A convenient approach for the synthesis of foldable redox-active flavin peptide conjugates was established. A model β-hairpin oligopeptide motif was utilized to demonstrate that azidolysine side-chains are readily functionalised with an alkyne-bearing flavine derivative. The folding equilibrium of the peptide backbone as well as the redox behaviour of the flavin moieties remains intact after the conjugation.

chemistry.chemical_classificationOligopeptideChemistryOrganic ChemistryPeptideFlavin groupBiochemistryRedoxCombinatorial chemistryFolding (chemistry)chemistry.chemical_compoundRedox activeheterocyclic compoundsPhysical and Theoretical ChemistryPeptidesDerivative (chemistry)Conjugate
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Vibronic structure in triatomic molecules : The hydrocarbon flame bands of the formyl radical (HCO). A theoretical study

1998

A theoretical study of the vibrational structure of the math 2A′ ground and math 2A′ excited states of the formyl radical, HCO, and its deuterated form, DCO, has been performed. The potential energy surfaces have been computed by means of a multiconfigurational perturbative method, CASPT2. The computed geometries and the harmonic and anharmonic frequencies are successfully compared to the available experimental information. The vibrational intensities of the transition math 2A′↔math 2A′ have been computed both for absorption and emission. The results lead to accurate determinations of several structural parameters and some reassignments of the vibrational transitions of the so-called hydroc…

chemistry.chemical_classificationOrganic compounds ; Free radicals ; Potential energy surfaces ; Vibronic states ; Vibrational statesChemistryTriatomic moleculeAnharmonicityGeneral Physics and AstronomyFree radicalsVibronic statesPotential energyUNESCO::FÍSICA::Química físicaHydrocarbonDeuteriumExcited statePotential energy surfacesOrganic compoundsVibrational statesPhysical and Theoretical ChemistryAbsorption (chemistry)Atomic physicsPhysics::Chemical Physics:FÍSICA::Química física [UNESCO]Astrophysics::Galaxy Astrophysics
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Contamination from polycyclic aromatic hydrocarbons (PAHs) in the soil of a botanic garden localized next to a former manufacturing gas plant in Pale…

2010

The Botanical Garden lies within the city of Palermo, a few meters away from one of the largest unused Manufacturing Gas Plant in Sicily. The total concentrations of PAHs (23 compounds) in the soil of Botanical Garden ranged from 947 to 18,072 microg/kg. The wide range of PAH concentrations (RSD=84%) found in the soil samples indicates heterogeneous levels of contamination in the area and this can be explained by considering the different tree distributions which prevents the homogeneous deposition of pollutants on the soil. Soils collected in the Botanical Garden generally showed the highest PAH concentrations, being almost 2-3 times higher than the concentration samples obtained in the ur…

chemistry.chemical_classificationPersistent organic pollutantEnvironmental EngineeringSoil testHealth Toxicology and MutagenesisGCMS Organic contaminants CarcinogeniMonitoring Botanic garden PalermoIndustrial WasteSoil classificationPollutionSoil contaminationSettore CHIM/12 - Chimica Dell'Ambiente E Dei Beni CulturaliDeposition (aerosol physics)chemistryItalyEnvironmental chemistrySoil waterEnvironmental ChemistryEnvironmental scienceSoil PollutantsOrganic matterBotanical gardenPolycyclic CompoundsGasesWaste Management and DisposalJournal of hazardous materials
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Does catalase play a role in Adriamycin induced cardiotoxicity?

1980

Summary Adriamycin causes an increase of lipid peroxidation in mouse cardiac homogenates that is dependent on the concentration of the antiblastic. The same phenomenon is not observed in the hearts of mice treated with an elevated dose of Adriamycin in which, conversely, an increase of the antioxidizing enzyme catalase was noticed. The significance of these findings is discussed with relationship to the hypothesis of an enhanced free radicals formation at the basis of Adriamycin induced cardiotoxicity.

chemistry.chemical_classificationPharmacologyCardiotoxicityLipid PeroxidesbiologyFree RadicalsHeart DiseasesMyocardiumPharmacologyNADCatalaseMalonatescarbohydrates (lipids)Lipid peroxidationchemistry.chemical_compoundMiceEnzymechemistryCatalaseDoxorubicinMalondialdehydepolycyclic compoundsbiology.proteinAnimalsFemalePharmacological Research Communications
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Propargyl-functional aliphatic polycarbonate obtained from carbon dioxide and glycidyl propargyl ether.

2013

The synthesis of propargyl-functional poly(carbonate)s with different content of glycidyl propargyl ether (GPE) units is achieved via the copolymerization of propargyl glycidyl ether and carbon dioxide. A new type of functional poly(carbonate) synthesized directly from CO(2) and the glycidyl ether is obtained. The resulting polymers show moderate polydispersities in the range of 1.6-2.5 and molecular weights in the range of 7000-10 500 g mol(-1). The synthesized copolymers with varying number of alkyne functionalities and benzyl azide are used for the copper-catalyzed Huisgen-1,3-dipolar addition. Moreover, the presence of vicinal alkyne groups opens a general pathway to produce functional …

chemistry.chemical_classificationPolycarboxylate CementPolymers and PlasticsOrganic ChemistryAlkynePolymerCarbon DioxideCatalysischemistry.chemical_compoundchemistryvisual_artPropargylPolymer chemistryMaterials ChemistryCopolymervisual_art.visual_art_mediumCarbonateOrganic chemistryEpoxy CompoundsAzidePolycarbonateVicinalCopperMacromolecular rapid communications
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Water-soluble hyperbranched polyglycerol photosensitizer for enhanced photodynamic therapy

2020

Porphyrin and its derivatives as promising photosensitizers have been widely utilized in photodynamic therapy (PDT). However, the water-solubility and biocompatibility of porphyrins are the typical bottlenecks in clinical PDT processes. Herein, we successfully fabricated a new type of water-soluble, hyperbranched polyglycerol photosensitizer through one-step esterification between water-soluble hyperbranched polyglycerol (hbPG) and fluorophenylporphyrin (FP). Compared with the linear control polymer, i.e., FP covalently connected with linear polyethylene glycol (LPEG), the hyperbranched structures bearing multiple porphyrin units generated more singlet oxygen and exhibited higher cytotoxici…

chemistry.chemical_classificationPolymers and PlasticsBiocompatibilitySinglet oxygenmedicine.medical_treatmentOrganic ChemistryBioengineeringPhotodynamic therapyPolymerBiochemistryCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryCovalent bondpolycyclic compoundsmedicinePhotosensitizerCytotoxicityPolymer Chemistry
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A Mixed-Ligand Approach for Spin-Crossover Modulation in a Linear FeII Coordination Polymer

2014

In this work, we present a family of Fe(II) coordination polymers of general formula [Fe(btzx)(3-3x)(btix)(3x)](ClO4)2 with interesting spin-crossover properties. These coordination polymers have been synthesized using chemical mixtures of two different but closely related ligands, 1,4-bis(tetrazol-1-ylmethyl)benzene (btzx) and 1,4-bis(triazol-1-ylmethyl)benzene (btix), and the effect of a gradual substitution of the ligand in the spin transition temperature has been investigated. Several chemical mixtures have been structurally characterized by X-ray powder diffraction indicating a clear critical amount in the composition of the mixture after which mixed phases rather than a single phase c…

chemistry.chemical_classificationPolymersChemistryCoordination polymerLigandStereochemistrySpin transitionPolymerLigands3. Good healthInorganic ChemistryThermogravimetrychemistry.chemical_compoundCrystallographySpin crossoverThermogravimetryFerrous CompoundsPhysical and Theoretical ChemistryBenzenePowder DiffractionPowder diffractionInorganic Chemistry
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ChemInform Abstract: Oppenauer Oxidation of Secondary Alcohols with 1,1,1-Trifluoroacetone as Hydride Acceptor.

2008

1,1,1-Trifluoroacetone (2a) reacts as a hydride-acceptor in the Oppenauer oxidation of secondary alcohols (1) in the presence of diethylethoxyaluminum. The oxidant allows for selective oxidation of secondary alcohols in the presence of primary alcohols.

chemistry.chemical_classificationPrimary (chemistry)HydrideChemistryOppenauer oxidationGeneral MedicineBridged compoundsMedicinal chemistryAcceptorChemInform
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Biopartitioning micellar chromatography: An alternative high-throughput method for assessing the ecotoxicity of anilines and phenols

2007

An investigation of the use of the chromatographic retention (log k) as an in vitro approach for modelling the toxicity to Fathead Minnows of anilines and phenols is developed. A data set of 65 compounds with available experimental toxicity data was used. Log k data at three pH values were used for the compounds classification and two groups or 'MODEs' were identified. For one 'MODE' a quantitative retention-activity relationship (QRAR) model was calculated. Finally, it was used to estimate the toxicity to Fathead minnows of anilines and phenols for which experimental data are not available. These estimations were compared to those obtained from another toxicity (to Tetrahymena pyriformis) …

chemistry.chemical_classificationQuantitative structure–activity relationshipAniline CompoundsChromatographyToxicity dataTetrahymena pyriformisClinical BiochemistryCyprinidaeQuantitative Structure-Activity RelationshipAromatic amineExperimental dataCell BiologyGeneral MedicineBiochemistryAnalytical Chemistrychemistry.chemical_compoundPhenolschemistryTetrahymena pyriformisToxicityAnimalsSpectrophotometry UltravioletPhenolsEcotoxicityChromatography Micellar Electrokinetic CapillaryJournal of Chromatography B
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