Search results for "ASTER"

showing 10 items of 2223 documents

Diagnostics applied to the finish decorative plaster. The case study of Santa Margherita di Belice

2013

Il terzo poster mostra il risultato delle applicazioni diagnostiche all'interno dell'ex Chiesa Madre di Santa Margherita di Belice (Agrigento). Poster number 3 presents the application of the diagnostic method on the plastered internal surfaces of the former Mother Church in Santa Margherita di Belice (Agrigento).

Diagnostica conservazione stuccoSettore ICAR/19 - RestauroDiagnostics conservation plaster
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Exploring theoretical frameworks for the analysis of fertility fluctuations

1988

The Easterlin theory, popular during the 1970s, explained population fluctuations in terms of maximization of choice, based on the evaluation of previously acquired information. Fluctuations in procreational patterns were seen as responses to conflict between 2 consecutive generations in which the propensity to procreate is inversely related to cohort size. However, the number of demographic trends not directly explainable by the hypothesis imply that either the model must be extended over a longer time frame or that there has been a drastic change of regime, i.e., a basic change in popular attitudes which determine decision making behavior. 4 strategic principles underlie reproductive deci…

DialecticBehaviorEconomicsMetaphorResearchmedia_common.quotation_subjectDecision MakingPopulation DynamicsSocial SciencesRationalityModels TheoreticalModels EconomicHuman geographyEconomicsEconomic modelNorm (social)Positive economicsSocial psychologyDemographyEasterlin hypothesismedia_commonPublic financeEuropean Journal of Population
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Chiral α-P,N Ligands From a Diastereoselective Ph2PH Addition to (η6-Benzaldimine)tricarbonylchromium Complexes

1999

International audience; Chiral α-aminophosphane (α-P–C–N) ligands have been prepared by reversible addition of Ph2PH to tricarbonylchromium benzaldimine complexes (CO)3Cr[η6-o-C6H4(Y)(CH=NR)] (with Y, R = CH3, CH3 or CH2COOCH3; CH3O, CH3 or p-CH3OC6H4; Cl, C6H5), with complete diastereoselectivity. These complexes are stabilized in solution by electron-withdrawing group(s) on the imine.

Diastereoselective reactionsStereochemistryOrganic ChemistryImine3. Good healthP ligandschemistry.chemical_compoundChromium complexeschemistryAminophosphaneGroup (periodic table)[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryChiralityChirality (chemistry)
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Synthesis of 8-aminomorphans with high KOR affinity

2021

2-Azabicyclo[3.3.1]nonanes (morphans) with a (3,4-dichlorophenyl)acetyl group at 2-position and a pyrrolidino moiety at 8-position were designed as conformationally restricted analogs of piperidine-based KOR agonists. The synthesis started with 4-oxopiperidine-2-carboxylic acid comprising 13 reaction steps. At first the ketone 10 was transformed into diester 7 bearing a propionate side chain. Dieckmann condensation of diester 7 to afford bicyclic enolester 14 and subsequent Krapcho deethoxycarbonylation represent the key steps of the synthesis. The enantiomeric pyrrolidines (1S,5R,8R)-5a and (1R,5S,8S)-5a were separated by chiral HPLC. The eutomer (1S,5R,8R)-5a showed high KOR affinity (K-i…

Diastereoselective reductive aminationEnantiomeric excessStructure-affinity relationshipsPharmacologyPyrrolidinesReceptors Opioid kappaNOESY spectrumOrganic ChemistryMolecular ConformationStereoisomerismGeneral MedicineKOR agonistsEndo-configurationStructure-Activity RelationshipKOR pharmacophoreConformational restrictionChiral HPLCDihedral angleDrug DiscoveryCis/trans-configurationMorphan2-azabicyclo[3.3.1]nonaneEuropean Journal of Medicinal Chemistry
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Addition of dianions of carboxylic acids to imines. Influence of the acid in the outcome of the reaction

2009

The addition of different carboxylic acids dianions to N-benzylidenebenzeneamine have been studied. The outcome of the reaction depends on the acid. Saturated ones lead to β-aminoacids with good yields and syn-selectivity whereas α,β-unsaturated ones lead to α− and γ− regioisomers with a regioselectivity that depends on the steric hindrance around the reactive centre. From some of these unsaturated acids, polyunsaturated carboxylic acids can be obtained as a change in the reaction conditions lead to the in situ elimination of aniline. From o-methyl aromatic acids δ-aminoacids are isolated with uneven results. Those derived from six member arene carboxylic acids give, on standing, dihydro-2-…

DiastereoselectivityDianions ; Imines ; Regioselectivity ; DiastereoselectivityDianionsRegioselectivityUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]IminesUNESCO::QUÍMICA::Química orgánica:QUÍMICA [UNESCO]
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Direct synthesis of C3-mono-functionalized oxindoles from N-unprotected 2-oxindole and their antileishmanial activity.

2014

A novel approach for the synthesis of unprecedented C3-mono-functionalized indolin-2-ones is reported, starting from 2-oxindole and chalcones. The reactions proceed regioselectively under mild conditions, without di- and tri-alkylated side products. The new compounds have been evaluated in vitro for their antiproliferative effects against the protozoan Leishmania infantum. Interestingly, they appear able to kill L. infantum promastigotes and amastigotes, without significant cytotoxic effects.

DiastereoselectivityLeishmanicidal activityIndolesStereochemistryClinical BiochemistryAntiprotozoal AgentsDrug Evaluation PreclinicalPharmaceutical Science2-oxindoleChemistry Techniques SyntheticBiochemistryCell LineMiceStructure-Activity RelationshipChalconeMichael additionparasitic diseasesDrug DiscoveryToxicity TestsAnimalsLeishmania infantumAmastigoteMolecular BiologyLeishmaniaOxindoles; Michael addition; Leishmania; Leishmanicidal activity; Diastereoselectivity; CyclizationbiologyDose-Response Relationship DrugChemistryOrganic Chemistrybiology.organism_classificationLeishmaniaCombinatorial chemistryIn vitroOxindolesCyclizationMichael reactionMolecular MedicineOxindoleLeishmania infantumBioorganicmedicinal chemistry
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Diastereoselective Synthesis of Dialkylated Bis(phosphino)ferrocenes: Their Use in Promoting Silver-Mediated Nucleophilic Fluorination of Chloroquino…

2017

International audience; The diastereoselective synthesis of dialkylated ferrocenyl bis(phosphane)s bearing aryl, alkyl, and hetero- or polycyclic substituents on the phosphino groups is reported, together with their characterization in the solid state by X-ray structure analysis and in solution by multinuclear NMR spectroscopy. Introduction of various alkyl groups on the ferrocene backbone, namely, tert-butyl, isopropyl, and trimethylsilyl, has a significant influence on the stereoselectivity of the ensuing lithiation/phosphination reactions. Only the introduction of the tert-butyl groups ensures both a high yield and perfect diastereoselectivity, which leads to the exclusive formation of t…

Diastereoselectivitybond formationTrimethylsilylfunctionalized arylone-potelectrophilic fluorinationPhosphanesAlkylationc-h fluorination[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundNucleophileFluorinationOrganic chemistryAlkylpolyphosphane ligandsferrocenyl derivativeschemistry.chemical_classificationp-31 nmr010405 organic chemistryArylHalex reactiondirect arylationreductive elimination[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryNuclear magnetic resonance spectroscopySandwich complexes0104 chemical scienceschemistryFerroceneIsopropyl
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Thermal, spectroscopic and crystallographic analysis of mannose-derived linear polyols

2018

The major diastereomer formed in the Barbier-type metal-mediated allylation of D-mannose has previously been shown to adopt a perfectly linear conformation, both in solid state and in solution, resulting in the formation of hydrogen-bonded networks and subsequent aggregation from aqueous solution upon stirring. Here, a comprehensive study of the solid state structure of both the allylated D-mannose and its racemic form has been conducted. The binary melting point diagram of the system was determined by differential scanning calorimetry analysis, and the obtained results, along with structure determination by single crystal X-ray diffraction, confirmed that allylated mannose forms a true rac…

DiffractionMaterials science010402 general chemistry01 natural sciencesDifferential scanning calorimetryNMR spectroscopycrystalsGeneral Materials SciencekalorimetriaNMR-spektroskopiata116x-ray crystallographyAqueous solution010405 organic chemistryDiastereomerGeneral ChemistryCondensed Matter Physicskiteet0104 chemical sciencessokerialkoholitCrystallographysugar alcoholsPolymorphism (materials science)Melting pointEnantiomerSingle crystalcalorimetryröntgenkristallografia
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High-energy X-ray diffraction and topography investigation of CdZnTe

2005

High-energy transmission x-ray diffraction techniques have been applied to investigate the crystal quality of CdZnTe (CZT). CdZnTe has shown excellent performance in hard x-ray and gamma detection; unfortunately, bulk nonuniformities still limit spectroscopic properties of CZT detectors. Collimated high-energy x-rays, produced by a superconducting wiggler at the National Synchrotron Light Source’s X17B1 beamline, allow for a nondestructive characterization of thick CZT samples (2–3 mm). In order to have complete information about the defect distribution and strains in the crystals, two series of experiments have been performed. First, a monochromatic 67 keV x-ray beam with the size of 300×3…

DiffractionMaterials sciencebusiness.industryWigglerSynchrotron radiationCondensed Matter PhysicsCollimated lightElectronic Optical and Magnetic MaterialsCrystalFull width at half maximumOpticsradiation detectorsBeamlineCadmium alloysMaterials ChemistryCadmium tellurideElectrical and Electronic EngineeringRaster scanbusinessJournal of Electronic Materials
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Synthesis and stereochemical studies of 1- and 2-phenyl-substituted 1,3-oxazino[4,3-a]isoquinoline derivatives

2003

Abstract Starting from the 1′- or 2′-phenyl-substituted 1-(2′-hydroxyethyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline diastereomers 3 and 6 , 4-unsubstituted and 4-(p-nitrophenyl)- and 4-oxo-substituted 1-phenyl- and 2-phenyl-9,10-dimethoxy-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinolines ( 7–12 ) were prepared. The relative configurations and the predominant conformations of the products were determined by NMR spectroscopy, by quantum chemical calculations and, for (2R∗,4S∗,11bR∗)-9,10-dimethoxy-4-(p-nitrophenyl)-2-phenyl-2H,4H-1,6,7,11b-tetrahydro-1,3-oxazino[4,3-a]isoquinoline ( 11 ), by X-ray diffraction.

DiffractionQuantum chemicalchemistry.chemical_classificationStereochemistryChemistryOrganic ChemistryDiastereomerOxazinesNuclear magnetic resonance spectroscopyBiochemistrychemistry.chemical_compoundComputational chemistryDrug DiscoveryIsoquinolineTetrahedron
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