Search results for "selectivity"

showing 10 items of 1148 documents

Food selectivity and pickiness in adulthood: an age and gender-related behaviour?

2013

Food pickiness –or selectivity- is a behavior which may lead to a lack of variety and an unbalanced diet. While this trait has been studied in children, pickiness in adults has been more rarely explored and only recently in French elderly1. The first aim of the present work was to identify if pickiness varies according to age and gender in adults. The second aim was to examine the link between the selectivity score and self-reported degree of pickiness. Four hundred French adults from 25 to 75 years old answered an online survey. Respondents were asked to tick each food they dislike among a list of 71 food items. The selectivity score was the number of disliked food items1. Moreover, partic…

[SDV.AEN] Life Sciences [q-bio]/Food and Nutritionadulthood[ SDV.AEN ] Life Sciences [q-bio]/Food and Nutritionfood selectivityage effectgenderpickiness[SDV.AEN]Life Sciences [q-bio]/Food and Nutrition
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The noncovalent dimerization of a G-quadruplex/hemin DNAzyme improves its biocatalytic properties.

2020

While many protein enzymes exert their functions through multimerization, which improves both selectivity and activity, this has not yet been demonstrated for other naturally occurring catalysts. Here, we report a multimerization effect applied to catalytic DNAs (or DNAzymes) and demonstrate that the enzymatic efficiency of G-quadruplexes (GQs) in interaction with the hemin cofactor is remarkably enhanced by homodimerization. The resulting non-covalent dimeric GQ–DNAzyme system provides hemin with a structurally defined active site in which both the cofactor (hemin) and the oxidant (H2O2) are activated. This new biocatalytic system efficiently performs peroxidase- and peroxygenase-type biot…

[SDV.BIO]Life Sciences [q-bio]/BiotechnologyDeoxyribozyme010402 general chemistryG-quadruplex01 natural sciencesCofactor03 medical and health scienceschemistry.chemical_compoundheterocyclic compounds030304 developmental biologychemistry.chemical_classification0303 health sciencesbiologyChemistryActive siteGeneral Chemistry[CHIM.CATA]Chemical Sciences/CatalysisCombinatorial chemistry[SDE.ES]Environmental Sciences/Environmental and Society0104 chemical sciencesChemistryEnzymebiology.proteinSelectivityPeroxidaseHeminChemical science
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Tuning the Basicity of Synergic Bimetallic Reagents: Switching the Regioselectivity of the Direct Dimetalation of Toluene from 2,5‐ to 3,5‐Positions

2008

Meta-meta metalation: Remarkably, toluene can be directly dimanganated or dimagnesiated at the 3,5-positions using bimetallic bases with active Me3SiCH2 ligands (see scheme, blue). In contrast, n-butyl ligands lead to 2,5-metalation (red). tmp=2,2,6,6-tetramethylpiperidide.

alkali metalsMetalationInorganic chemistrychemistry.chemical_elementManganesemetalationmagnesium010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundinverse crown compoundsBimetallic strip010405 organic chemistryRegioselectivityGeneral ChemistryGeneral MedicineAlkali metalCombinatorial chemistryTolueneCommunications3. Good health0104 chemical scienceschemistryReagentmanganeseAngewandte Chemie
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Efficient synthesis of new C-functionalized macrocyclic polyamines

2010

A powerful synthetic route for the preparation of new poly-azamacrocycles, valuable precursors of bifunctional chelating agents with applications in nuclear medicine, is reported. The desired functional group was introduced onto the macro-cycle backbone during the cyclization step, thus avoiding the tedious preparation of a C-functionalized synthon. The regioselective reaction of macrocycles bearing an aminomethyl pendant arm with aldehydes is also described.

amines010402 general chemistry01 natural sciencesAldehydeChemical synthesischemistry.chemical_compoundN ligands[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalComputingMilieux_MISCELLANEOUSchemistry.chemical_classification010405 organic chemistryLigand[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistrySynthonRegioselectivity0104 chemical sciences3. Good healthmacrocycleschemistryFunctional groupbifunctional chelating agents
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Unveiling the Different Reactivity of Bent and Linear Three-Atom-Components Participating in [3 + 2] Cycloaddition Reactions

2021

The reactivity of a series of pairs of bent and linear three-atom-component (B-TACs and L-TACs) participating in [3 + 2] cycloaddition (32CA) reactions towards ethylene and electrophilic dicyanoethylene (DCE) have been studied within the Molecular Electron Density Theory. While the pseudodiradical structure of B-TACs changes to that of pseudoradical or carbenoid L-TACs upon dehydrogenation, zwitterionic B-TACs remain unchanged. Conceptual Density Functional Theory (CDFT) indices characterize five of the nine TACs as strong nucleophiles participating in polar reactions towards electrophilic ethylenes. The activation energies of the 32CA reactions with electrophilic DCE range from 0.5 to 22.0…

analytical_chemistry[3 + 2] cycloaddition reactionsOrganic chemistrychemical and pharmacologic phenomena010402 general chemistry01 natural sciencesQD241-441stomatognathic systemNucleophileComputational chemistrySingle bondReactivity (chemistry)skin and connective tissue diseasesCarbenoid010405 organic chemistryChemistrymolecular electron density theoryRegioselectivity16. Peace & justiceCycloaddition0104 chemical sciencesreactivitystomatognathic diseasesbent and linear three-atom-componentsregioselectivityElectrophileDensity functional theoryOrganics
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Chiral hemicucurbit[8]uril as an anion receptor: selectivity to size, shape and charge distribution

2017

A novel eight-membered macrocycle of the hemicucurbit[n]uril family, chiral (all-R)-cyclohexanohemicucurbit[8]uril (cycHC[8]) binds anions in a purely protic solvent with remarkable selectivity. The cycHC[8] portals open and close to fully encapsulate anions in a 1 : 1 ratio, resembling a molecular Pac-Man™. Comprehensive gas, solution and solid phase studies prove that the binding is governed by the size, shape and charge distribution of the bound anion. Gas phase studies show an order of SbF6− ≈ PF6− > ReO4− > ClO4− > SCN− > BF4− > HSO4− > CF3SO3− for anion complexation strength. An extensive crystallographic study reveals the preferred orientations of the anions within the octahedral cav…

anion receptors010405 organic chemistryStereochemistryselectivityCharge densityIsothermal titration calorimetryGeneral Chemistryhemicucurbituril010402 general chemistry01 natural sciences0104 chemical sciencesIonSolventCrystallographychemistry.chemical_compoundmacrocyclesOctahedronchemistryPhase (matter)Selectivityta116Protic solventChemical Science
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1-methil-3H-pyrazolo[1-2-a]benzo[1-2-3-4]tetrazin-3-ones, design synthesis and biological activity of new antitumoral agents

2005

1-Methylpyrazolo[1,2-a]benzo[1,2,3,4]tetrazin-3-ones 4, synthesized in good to excellent yields, were designed as novel alkylating agents because of their peculiar chemical behavior. All derivatives showed antiproliferative activity against more than 50 types of tumor cell lines with GI50 reaching sub-micromolar values. SAR studies revealed that the presence of a chlorine atom is well-tolerated in both positions 8 and 9, whereas in the case of the methyl group, switching from the 8 to the 9 position gives rise to the most active compound of the series, 4g, either for the number of cell lines inhibited and for selectivity against leukaemia and renal cancer subpanels. COMPARE and 3D-MIND comp…

antiproliferative activityQuantitative structure–activity relationshipStereochemistry2-a]benzotetrazinoneQuantitative Structure-Activity RelationshipRifamycinsAntineoplastic Agents1-Methylpyrazolo[12-a]benzo[1234]tetrazin-3-oneChemical synthesischemistry.chemical_compoundantiproliferativeCell Line TumorDrug DiscoveryCOMPARE and 3D-MIND analysisHumansComputer Simulationpyrazolo[1CytotoxicityBiological activityCytidinechemistryDrug Designantitumor agentMolecular MedicinePyrazolesDrug Screening Assays AntitumorSelectivityHeterocyclic Compounds 3-RingMethyl group
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Badanie selektywności systemu podatkowego stanowiącego program pomocy – glosa do wyroku TSUE z dnia 16 marca 2021 r. w sprawie C-562/19 P Komisja Eur…

2021

Niniejszy artykuł ma na celu przedstawienie zagadnienia sposobu badania selektywności programu pomocy, który jest środkiem pomocy państwa w rozumieniu art. 107 ust. 1 Traktatu o funkcjonowaniu Unii Europejskiej1. Jednocześnie praca ta stanowi glosę do obecnie najnowszej wypowiedzi TSUE w tym przedmiocie, czyli do wyroku z dnia 16 marca 2021 r. w sprawie C-562/19 P Komisja Europejska v. Rzeczpospolita Polska2 (podatek od sprzedaży detalicznej), wraz z omówieniem dotychczasowego dorobku orzecznictwa. Artykuł odnosi się do stanu prawa i orzecznictwa na dzień 31 marca 2021 r.

art. 107 ust. 1 TFUEArticle 107 (1) TFEUsystem podatkowypodatek od sprzedaży detalicznejselectivityselektywnośćsystem of taxationPolish tax on the ret ail sectorState aidpomoc państwaDoradztwo Podatkowe Biuletyn Instytutu Studiów Podatkowych
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Selective derivatisation of resorcarenes: 1. The regioselective formation of tetra-benzoxazine derivatives

1997

Abstract Four 5,6-benzo-1,3-oxazine rings are formed by the condensation of resorcarenes with various aliphatic or aromatic primary amines and formaldehyde. From four possible regioisomers only the C4 symmetrical compound is isolated in yields of up to 90%. Semiempirical calculations confirm its relative stability, which is due to the possible formation of four intramolecular OH…O hydrogen bonds. The regioselectivity of the reaction is further established for two examples by single crystal X-ray analysis. A solvent molecule is included in the extended cavity.

biologyChemistryHydrogen bondOrganic ChemistryCondensationFormaldehydeRegioselectivitybiology.organism_classificationBiochemistryMedicinal chemistrychemistry.chemical_compoundIntramolecular forceDrug DiscoveryStructural isomerTetraOrganic chemistrySingle crystalTetrahedron
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A remarkable selectivity in the N-functionalization of polyaza[n]paracyclophanes. Synthesis of N-(4-picolyl)-substituted 2,6,9,13-tetraaza[14]paracyc…

1997

Abstract Interaction of cationic host species, in particular Zn 2+ salts, with polyaza[n]paracyclophanes (i.e. 2,6,9,13-Tetraaza[14]paracyclophane, B323 (1a) ) directs their selective N-functionalization. In this way compounds mono- or difunctionalized with ArCH 2− groups at the benzylic nitrogen atoms can be easily obtained. Direct reaction with the alkylating agent, in the absence of the Zn 2+ species, produces, in general, very complex mixtures of mono- and polyalkylated compounds except when 4-picolyl chloride is used. In this case, mono-, di-, tri- and tetra N-substituted derivatives of D323 can be isolated depending on the amount of the alkylating agent used. In this case, the mono- a…

biologyChemistryStereochemistryOrganic ChemistryCationic polymerizationchemistry.chemical_elementbiology.organism_classificationBiochemistryMedicinal chemistryChlorideNitrogenMetalvisual_artDrug Discoverymedicinevisual_art.visual_art_mediumTetraSurface modificationDirect reactionSelectivitymedicine.drug
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