Search results for "Conjugate"

showing 10 items of 644 documents

Free and conjugated polyamine content in Citrus sinensis Osbeck, cultivar Brasiliano N.L.92, a Navel orange, at different maturation stages

2004

Biogenic amines, synthesized during physiological metabolic processes of all living organisms, are present in food. At low concentrations, polyamines are essential for cell renewal and growth, but they can be detrimental when consumed in high amount through the diet as they could support abnormal cell growth pathologies. The daily human diet contains more putrescine than spermidine or spermine, mostly derived from fruits. In general, orange fruits contain high levels of put, a fact that could limit their utilization in the daily diet besides the benefits contributed by their strong antioxidant properties. There is therefore an increasing interest in finding plant foods with low polyamine co…

biologySperminefood and beveragesGeneral MedicineOrange (colour)biology.organism_classificationAnalytical ChemistrySettore AGR/03 - Arboricoltura Generale E Coltivazioni ArboreeSpermidinechemistry.chemical_compoundRutaceaechemistryPolyamines Orange Spermidine Putrescine Conjugated polyaminesBotanyPutrescineFood scienceCultivarPolyamineCitrus × sinensisFood Science
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The Structural Diversity of Benzofuran Resorcinarene Leads to Enhanced Fluorescence

2014

An unexpected and previously unknown resorcinarene mono-crown with a fused benzofuran moiety in its macrocyclic core was obtained as a byproduct from a bridging reaction of tetramethoxy resorcinarene with tetraethylene glycol ditosylate. The formation of the fused benzofuran moiety in the resorcinarene macrocycle resulted in a unique rigid and puckered boat conformation, as shown by XRD studies in the solid state. Modification of the macrocycle was also observed to affect the photophysical properties in solution by enhancing the fluorescence brightness compared with a conventional resorcinarene macrocycle. The fluorescent properties enabled unique detection of structural features, that is, …

calixarenesStereochemistryPhenylalanineCyclohexane conformationMolecular ConformationSupramolecular chemistryChemistry Techniques SyntheticConjugated systemCrystallography X-RayBiochemistrysupramolecular chemistryStructure-Activity Relationshipchemistry.chemical_compoundCalixarenePolymer chemistrysupramolekulaarinen kemiaresorcinarenesMoietyBenzofuranX-ray diffractta116BenzofuransMolecular StructureOrganic Chemistryfluoresenssita1182benzofuranGeneral ChemistryResorcinareneFluorescenceX-ray diffractionSpectrometry FluorescencechemistryfluorescenceChemistry - An Asian Journal
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Copper-Catalyzed One-Pot Synthesis of 3-(N -Heteroarenyl)acrylonitriles through Radical Conjugated Addition of β-Nitrostyrene to Methylazaarenes

2020

chemistryOrganic ChemistryOne-pot synthesisPolymer chemistryCopper catalyzedchemistry.chemical_elementPhysical and Theoretical ChemistryConjugated systemCopperEuropean Journal of Organic Chemistry
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ChemInform Abstract: Conjugate Addition of Organolithium Reagents to α,β-Unsaturated Carboxylic Acids.

2010

Abstract Conjugate addition of primary, secondary, tertiary alkyl and phenyl lithium reagents to 2-alkenoic acids affords good yields of branched saturated carboxylic acids. Methyl groups at the α- and β-carbon of the 2-alkenoic acid decrease reactivity as acceptors, and foster deprotonation, respectively. The lithium enediolate resulting from the conjugate addition can react with electrophiles. PM3 calculations are in agreement with the substituent effects.

chemistry.chemical_classificationAddition reactionSubstituentchemistry.chemical_elementGeneral MedicineMedicinal chemistrychemistry.chemical_compoundDeprotonationchemistryElectrophileOrganic chemistryLithiumReactivity (chemistry)AlkylConjugateChemInform
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Stereoselective Conjugate Addition of Mixed Organoaluminum Reagents to ?,?-Unsaturated N-Acyloxazolidinones Derived from Carbohydrates.

2005

The stereoselective synthesis of β-branched carboxylic acid derivatives was accomplished by conjugate addition of mixed organoaluminum reagents to chiral α,β-unsaturated N-acyloxazolidinones. Mixed organoaluminum reagentswere generated in situ by transmetalation of Grignard or organolithium compounds with methylaluminum dichloride. Efficient stereocontrol was achieved using different bicyclic glycosamine-derived oxazolidinones, yielding alternatively (R)- or (S)-configured β-branched carboxylic acid derivatives.

chemistry.chemical_classificationAddition reactionTransmetalationchemistryBicyclic moleculeOrganolithium compoundsReagentCarboxylic acidOrganic chemistryStereoselectivityGeneral MedicineConjugateChemInform
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Cycloalkin-vinylidencycloalkan-umlagerungen

1989

Abstract Flash pyrolysis of the strained cyclic alkynes 1 leads to ring systems 2 with an exocyclic allene group and in a further isomerization step to the conjugated vinyl compounds 3 .

chemistry.chemical_classificationAlleneOrganic ChemistryConjugated systemRing (chemistry)PhotochemistryBiochemistryMedicinal chemistrychemistry.chemical_compoundHydrocarbonchemistryDrug DiscoveryIsomerizationPyrolysisTetrahedron Letters
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Anthracene Based Conjugated Polymers: Correlation between π−π-Stacking Ability, Photophysical Properties, Charge Carrier Mobility, and Photovoltaic P…

2010

This article reports on the synthesis, characterization and properties of a series of anthracene−containing poly(p-phenylene-ethynylene)-alt-poly(p-phenylene-vinylene)s (PPE−PPV) copolymers with general constitutional unit (Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n denoted AnE-PV. Solely linear (AnE-PVaa, -ad, -ae) and solely branched (AnE-PVbb) as well as mixed linear and branched (AnE-PVab, -ac, -ba, -cc) alkoxy side chains were grafted to the backbone in order to tune the π−π-stacking ability of the materials. It has been possible to establish a correlation between π−π-stacking ability, absorptive behavior, charge carrier mobility, solar cell active layer nanoscale morphology and resulting p…

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsOpen-circuit voltageOrganic ChemistryStackingPolymerConjugated systemlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawSolar cellPolymer chemistryMaterials ChemistrySide chainAlkoxy groupMacromolecules
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Intercorrelation between Structural Ordering and Emission Properties in Photoconducting Polymers

2009

We investigated the structural properties of anthracene containing poly(p-phenylene−ethynylene)-alt-poly(p-phenylene−vinylene) polymers with general constitutional unit: (−Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n by means of wide-angle X-ray scattering and fluorescence spectroscopy. Interchain interactions were systematically modified by decorating the conjugated polymer backbone with linear or branched or combinations of linear and branched alkoxy side chains. Special emphasis is taken on an evaluation method for fiber scattering spectra that allows the deduction of important structural details of polymer materials with limited degree of order. These include positional correlations along the …

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsScatteringOrganic ChemistryStackingPolymerConjugated systemFluorescence spectroscopyInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryAlkoxy groupSide chainMacromolecules
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[39] Lipoperoxyl radical-scavenging activity of vitamin A and analogs in homogeneous solution

1994

Publisher Summary This chapter describes the assay method for determining the reactivity of all- trans -retinol and other natural and synthetic retinoids, with radicals generated by reaction of the lipid-soluble azo initiator 2,2 ' -azobis(2,4-dimethylvaleronitrile) (AMVN) with methyl linoleate. The chapter discusses the general principles for measuring antioxidant activity. The oxidation of linoleic acid methyl ester (LAME) is the simplest model for studying the oxidation of polyunsaturated lipids and has been widely adopted to evaluate antioxidant activity. Because linoleic acid has two double bonds, peroxidation occurs at the bisallylic hydrogens and generates conjugated diene hydroperox…

chemistry.chemical_classificationAntioxidantDouble bondLinoleic acidmedicine.medical_treatmentRadicalSubstrate (chemistry)Conjugated systemchemistry.chemical_compoundchemistryLipid oxidationmedicineOrganic chemistryReactivity (chemistry)
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Structural Characterization of Glycoconjugate Polystyrene in Aqueous Solution

1999

Maltopentaose-carrying polystyrene was synthesized by the homopolymerization of vinylbenzyl maltopentaose amide. Resulted amphiphilc polymacromonomer was dissolved in 0.1 M urea aqueous solution, and its structure was characterized by small-angle X-ray scattering and molecular modeling. Maltopentaose-carrying polystyrene polymacromonomer was found to be represented by a molecular bottlebrush, composed of a large helix of polystyrene backbone and maltopentaose brushes. The molecular bottlebrush seems to be distributed randomly or many even be broken once or twice in segments with no apparent intersegmental spatial correlation. A large helix of polystyrene backbone is formed by a random seque…

chemistry.chemical_classificationAqueous solutionPolymers and PlasticsMolecular modelGlycoconjugateOrganic ChemistryRadical polymerizationInorganic Chemistrychemistry.chemical_compoundAldosechemistryAmidePolymer chemistryMaterials ChemistryUreaPolystyreneMacromolecules
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