Search results for "aroma"

showing 10 items of 1006 documents

Evaluation of the aroma compounds of Sicilian Cactus pear (Opuntia Ficus-Indica) fermented juice

2011

aroma compounds fermented juice Opuntia Ficus-Indica)Settore AGR/15 - Scienze E Tecnologie Alimentari
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Investigating the effect of meat products ingredients and reaction mechanisms for enchancing savory and toasted aromas in dry cured meat products

2023

En la carne cocinada, las notas olfativas cárnicas y tostadas son producidas mediante reacciones de degradación y transformación de aminoácidos que contienen átomos de azufre (Cys, Cis y Met), aminoácidos nitrogenados (Pro y Orn), así como de la vitamina tiamina. Sin embargo, en los productos curados madurados no se conocen los mecanismos de formación de los compuestos aromáticos que producen notas cárnicas y tostadas, así como su impacto en el aroma curado-madurado. Entre los productos cárnicos curados madurados que se elaboran en el área mediterránea se encuentran los sometidos a procesos de fermentación como los embutidos fermentados, y los curados-madurados como los lomos y jamones cura…

aromadry cured meatUNESCO::CIENCIAS TECNOLÓGICAS::Tecnología de los alimentos
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Desarrollo de embutidos con menores niveles de nitrificantes inoculados con levaduras seleccionadas para mantener las características sensoriales pro…

2020

Los agentes de curado (nitratos y nitritos) desempeñan funciones importantes en la elaboración de embutidos curado-madurados, entre las que se encuentra el desarrollo del aroma característico de estos productos. El uso exclusivo de nitrato, de nitrito o de una mezcla de los dos, puede tener diferente repercusión en el perfil aromático. Sin embargo, existe una tendencia a la reducción del uso de estos aditivos por su relación con la generación de N-nitrosaminas que ha hecho que en los últimos años exista una gran preocupación a nivel de los consumidores. Por ello, en la presente tesis doctoral se ha estudiado el efecto que produce la reducción de la cantidad añadida de nitrato o de la mezcla…

aromaembutidos curado-maduradosreducción de nitrificantesUNESCO::CIENCIAS MÉDICASnitritocompuestos volátiles:CIENCIAS AGRARIAS [UNESCO]:CIENCIAS MÉDICAS [UNESCO]nitratoUNESCO::CIENCIAS AGRARIAS
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Asymmetric synthesis of functionalized tetrahydrofluorenones via an NHC-catalyzed homoenolate Michael addition

2018

The first example of an N-heterocyclic carbene-catalyzed asymmetric desymmetrization of enal-tethered cyclohexadienones via an intramolecular homoenolate Michael addition/esterification reaction is described. This new protocol offers a direct entry to various functionalized tetrahydrofluorenones with three contiguous stereocenters in high yields, good diastereoselectivities and excellent enantioselectivities.

aromaattiset yhdisteet010402 general chemistry01 natural sciencesDesymmetrizationCatalysisStereocenterCatalysisDirect entryMaterials Chemistryta116kemiallinen synteesi010405 organic chemistryChemistryaromatic compoundsMetals and AlloysEnantioselective synthesisGeneral ChemistryCombinatorial chemistry0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsIntramolecular forceCeramics and CompositesMichael reactionEsterification reactionchemical synthesisChemical Communications
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Fluorescence enhancement of quinolines by protonation.

2020

A study of the fluorescence enhancement of isoquinoline, acridine (benzo[b]quinoline) and benzo[h]quinoline is reported with six organic acids of different pKa values. Protonation was found to be an effective tool in the fluorescence enhancement of quinolines. A significant increase in the fluorescence intensity is observed only when strong acids are used, resulting in an over 50-fold increase in fluorescence with trifluoroacetic or benzenesulfonic acid and isoquinoline in a 1.5 : 1 ratio. The benzenesulfonic acid was found to be the most effective in the protonation of the bases despite its higher pKa value compared to trifluoro- and trichloroacetic acid. The X-ray crystal structures of 14…

aromaattiset yhdisteet010405 organic chemistryHydrogen bondprotonationGeneral Chemical Engineering116 Chemical sciencesQuinolinefluoresenssifluorescence enhancementProtonationGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryFluorescence3. Good health0104 chemical scienceschemistry.chemical_compoundBenzenesulfonic acidchemistryAcridineTrichloroacetic acidIsoquinolineRSC advances
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Nonlinear optical properties of diaromatic stilbene, butadiene and thiophene derivatives

2021

Series of highly polar stilbene (1a–e), diphenylbutadiene (2a–c) and phenylethenylthiophene (3a–c) derivatives were prepared via Horner–Wadsworth–Emmons method with a view to produce new and efficient materials for second harmonic generation (SHG) in the solid-state. The single-crystal X-ray structures of compounds 1–3 reveal extensive polymorphism and a peculiar photodimerization of the 2-chloro-3,4-dimethoxy-4′-nitrostilbene derivative 1a to afford two polymorphs of tetra-aryl cyclobutane 4. The stilbene congeners 2-chloro-3,4-dimethoxy-4′-nitrostilbene (1a·non-centro), 5-bromo-2-hydroxy-3-nitro-4′-nitrostilbene (1b) and 4-dimethylamino-4′-nitrostilbene (1e), as well as 4′-fluoro-4′′-nitr…

aromaattiset yhdisteet010405 organic chemistrySecond-harmonic generationbutadieeniGeneral ChemistryConjugated systemChromophoreoptiset ominaisuudetkiteet010402 general chemistry01 natural sciencesFluorescenceCatalysis0104 chemical sciencesCyclobutaneCrystallographychemistry.chemical_compoundNonlinear opticalPolymorphism (materials science)chemistrystilbeenitMaterials ChemistryUreaorgaaniset yhdisteetNew Journal of Chemistry
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Towards low-energy-light-driven bistable photoswitches : ortho-fluoroaminoazobenzenes

2021

AbstractThermally stable photoswitches that are driven with low-energy light are rare, yet crucial for extending the applicability of photoresponsive molecules and materials towards, e.g., living systems. Combined ortho-fluorination and -amination couples high visible light absorptivity of o-aminoazobenzenes with the extraordinary bistability of o-fluoroazobenzenes. Herein, we report a library of easily accessible o-aminofluoroazobenzenes and establish structure–property relationships regarding spectral qualities, visible light isomerization efficiency and thermal stability of the cis-isomer with respect to the degree of o-substitution and choice of amino substituent. We rationalize the exp…

aromaattiset yhdisteetMaterials sciencephotochemistryBistabilityLightbusiness.industry010405 organic chemistry116 Chemical sciences010402 general chemistry01 natural sciencesfluori0104 chemical sciencesLow energyIsomerismLight drivenOptoelectronicsvalokemiaPhysical and Theoretical Chemistrybusiness
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Design, Construction, and Characterization of a New Regioisomer and Diastereomer Material Based on the Spirooxindole Scaffold Incorporating a Sulphon…

2020

The 1,3-dipolar cycloaddition reaction is one of the most rapid, and efficient protocols to access, and construct highly divergent heterocycle chiral auxiliaries. Free catalyst synthesis of spirooxindole scaffold incorporating sulphone moiety via one pot&ndash

aromaattiset yhdisteetPhysics and Astronomy (miscellaneous)isomeriaGeneral Mathematics13-dipolar cycloaddition reaction010402 general chemistry01 natural sciencesdiastereomerComputational chemistrysulphonerikkiyhdisteetComputer Science (miscellaneous)MoietyReactivity (chemistry)Molecular orbitalHOMO/LUMOorgaaniset yhdisteet010405 organic chemistryChemistrylcsh:MathematicsChemical shiftDiastereomerspirooxindoleHirshfeld analysislcsh:QA1-939Cycloaddition0104 chemical sciencesregioisomerChemistry (miscellaneous)Natural bond orbitalSymmetry
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Mono-nitrotolueenien muuntuminen

2008

aromaattiset yhdisteethapetussonolyysiotsoninitrotolueenibiohajoaminenFentonin reagenssi
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Synthesis of N‐Fused Indolines via Copper (II)‐Catalyzed Dearomatizing Cyclization of Indoles

2021

Advanced synthesis & catalysis 363(12), 3121-3126 (2021). doi:10.1002/adsc.202100290

aromaattiset yhdisteetkemiallinen synteesi660Chemistrychemistry.chemical_elementkupariGeneral ChemistryMedicinal chemistryCopperCatalysischemistry.chemical_compoundkatalyysiIndolineddc:660orgaaniset yhdisteet
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