Search results for "Reagent"

showing 10 items of 699 documents

Ageing behaviour and analytical characterization of the Jatobá resin collected from Hymenaea stigonocarpa Mart.

2009

Abstract This paper reports the results of an analytical study to characterize the trunk resin collected from the Hymenaea stigonocarpa Mart. species from the region of Minas Gerais (Brazil), popularly known as Jatoba resin. Hymenaea resins are reported to have been used in artistic applications such as protective varnishes in polychromed sculptures and paintings. Therefore, the identification of the main chemical changes that take place in the resin when it is prepared as a thin film exposed to atmospheric effects have been considered herein. Changes due to the degradation effect of light have been studied on a series of specimens prepared as a thin films and subjected to accelerated UV li…

food.ingredientChromatographybiologyChemistryVarnishCondensed Matter Physicsbiology.organism_classificationCopalic acidchemistry.chemical_compoundfoodAgeingReagentvisual_artvisual_art.visual_art_mediumHymenaeaPhysical and Theoretical ChemistryHymenaea stigonocarpaGas chromatography–mass spectrometryDerivatizationInstrumentationSpectroscopyInternational Journal of Mass Spectrometry
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Recent advances in the application of microbial transglutaminase crosslinking in cheese and ice cream products: A review

2018

Microbial transglutaminase (MTGase) has been currently utilized to form new food structures and matrices with high physicochemical stability. Incorporation of this multi-functional enzyme into structural composition of milk protein-based products, such as cheese and ice cream, can not only be a successful strategy to improve their nutritional and technological characteristics through intramolecular cross-linking, but also to reduce the production cost by decreasing fat and stabilizer contents. The recent research developments and promising results of MTGase application in producing functional formulations of cheese and ice cream with higher quality characteristics are reviewed. New interest…

food.ingredientFood HandlingOrganolepticBiochemistry0404 agricultural biotechnologyfoodCheeseStructural BiologyEnzyme StabilityAnimalsHumans[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringFood scienceMolecular Biology2. Zero hungerTransglutaminasesMoisture[SDE.IE]Environmental Sciences/Environmental EngineeringChemistryIce CreamFood additivefood and beveragesFood composition data04 agricultural and veterinary sciencesGeneral MedicineMilk Proteins040401 food scienceCross-Linking ReagentsWhey ProteinsIce creamFood TechnologyFood qualityMicrobial transglutaminaseStabilizer (chemistry)International Journal of Biological Macromolecules
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Acylative Dynamic Kinetic Resolution of Secondary Alcohols: Tandem Catalysis by HyperBTM and Bäckvall's Ruthenium Complex.

2021

Non-enzymatic dynamic kinetic resolution (DKR) of secondary alcohols by enantioselective acylation using an isothiourea-derived HyperBTM catalyst and racemization of slowly reacting alcohol by Backvall's ruthenium complex is reported. The DKR approach features high enantioselectivities (up to 99:1), employs easy-to-handle crystalline 4-nitrophenyl isobutyrate as the acylating reagent, and proceeds at room temperature and under an ambient atmosphere. The stereoinduction model featuring cation-π system interactions between the acylated HyperBTM catalyst and π electrons of an alcohol aryl subunit has been elaborated by DFT calculations.

inorganic chemicals010405 organic chemistryArylOrganic ChemistryEnantioselective synthesischemistry.chemical_elementStereoisomerism010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisRuthenium0104 chemical sciencesRutheniumCatalysisKinetic resolutionAcylationchemistry.chemical_compoundKineticschemistryReagentAlcoholsRacemizationThe Journal of organic chemistry
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More than a Confinement: “Soft” and “Hard” Enzyme Entrapment Modulates Biological Catalyst Function

2019

Catalysis makes chemical and biochemical reactions kinetically accessible. From a technological point of view, organic, inorganic, and biochemical catalysis is relevant for several applications, from industrial synthesis to biomedical, material, and food sciences. A heterogeneous catalyst, i.e., a catalyst confined in a different phase with respect to the reagents’ phase, requires either its physical confinement in an immobilization matrix or its physical adsorption on a surface. In this review, we will focus on the immobilization of biological catalysts, i.e., enzymes, by comparing hard and soft immobilization matrices and their effect on the modulation of the catalysts’ function. Indeed, …

inorganic chemicals02 engineering and technology010402 general chemistryHeterogeneous catalysisbiosensor01 natural sciencesCatalysischemistry.chemical_compoundbioreactorAdsorptionBioreactorMoleculePhysical and Theoretical ChemistrytrehalosecatalysisSilica gelsilica gel021001 nanoscience & nanotechnology0104 chemical sciencesenzymeChemical engineeringchemistryReagentencapsulation0210 nano-technologyBiosensor
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Dual stereocontrolled alkylation of aldehydes with polystyrene-supported nickel complexes derived from α-amino amides

2015

Nickel(II) complexes derived from α-amino amide ligands anchored to gel-type and monolithic polymers act as efficient catalysts for the enantioselective addition of dialkylzinc reagents to aldehydes. Similar to the analogous homogeneous systems, dual stereocontrol in addition products can be achieved by controlling the stoichiometry of the immobilized nickel complex. Aromatic and aliphatic aldehydes were alkylated in good yields with enantioselectivities comparable to those obtained with the homogeneous analogues. These polymer-supported catalysts offer significant advantages as no metal leaching is observed and they can be easily recovered from the reaction mixture by simple filtration and…

inorganic chemicalsAldehydesCatalystsGeneral Chemical EngineeringPolymer supported catalystsEnantioselective synthesischemistry.chemical_elementEnantioselectivityGeneral ChemistryAlkylationAmidesCatalysischemistry.chemical_compoundNickelchemistryCatàlisiNickelAmideReagentOrganic chemistryPolystyreneQuímica orgànicaStoichiometry
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Determination of Cd, Co, Cu, Fe, Pb, Mn, Ni and Zn in diets: Development of a method

1991

A method useful for the determination of cadmium, cobalt, copper, iron, lead, manganese, nickel and zinc in diets is described. Organic matter is destroyed applying a wet procedure, and element content is measured by flame atomic absorption spectroscopy (FAAS) in the case of copper, iron, manganese, nickel and zinc, and by graphite furnace (GF-AAS) in the case of cadmium, cobalt and lead. The matrix interference study is carried out. Values found for linearity, detection and quantitation limits as well as accuracy show that the described method is useful to determine the elements taken into account at usual levels in diets.

inorganic chemicalsCadmiumSpectrophotometry AtomicMetallurgychemistry.chemical_elementManganeseZincCopperlaw.inventionNickelchemistryMetalslawIndicators and ReagentsGraphiteAtomic absorption spectroscopyCobaltFood AnalysisFood ScienceNuclear chemistryFood / Nahrung
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Gravimetric determination of palladium with biguanide sulfate

1986

Abstract Biguanides are interesting reagents for the determination of palladium owing to their solubility, chemical resistance, and selectivity in moderately acidic solutions. A procedure for the gravimetric determination of palladium(II) in the form of Pd(HL)2SO4, where HL = biguanide, is proposed and the conditions of precipitation, treatment of the precipitate, precision, accuracy, and selectivity of the procedure are discussed.

inorganic chemicalsChemical resistanceChemistryPrecipitation (chemistry)Inorganic chemistrychemistry.chemical_elementAnalytical Chemistrychemistry.chemical_compoundReagentGravimetric analysisSolubilitySulfateSelectivitySpectroscopyPalladiumMicrochemical Journal
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Preparation of 2,3-seco-5α-cholestane-2,3-diol and 4α-methyl-2,3-seco-5α-cholestane-2,3-diol and its reactions with o-nitrophenyl selenocyanate

1984

The reaction of 2,3-seco-5 alpha-cholestane-2,3-diol and 4 alpha-methyl-2,3-seco-5 alpha-cholestane-2,3-diol with o-nitrophenyl selenocyanate was studied. The diols were synthesized from cholesterol.

inorganic chemicalsMagnetic Resonance SpectroscopyChemical PhenomenaOptical RotationSpectrophotometry InfraredClinical BiochemistryDiolBiochemistrychemistry.chemical_compoundEndocrinologySpectrophotometryNitrilespolycyclic compoundsmedicineSecosteroidsOrganic chemistryMolecular BiologyPharmacologyintegumentary systemmedicine.diagnostic_testorganic chemicalsOrganic ChemistryNuclear magnetic resonance spectroscopyChemistrychemistryIndicators and ReagentsCholestaneCholestanolshormones hormone substitutes and hormone antagonistsSteroids
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Thieme Chemistry Journals Awardees – Where Are They Now? Molybdenum(V)-Mediated Synthesis of Nonsymmetric Diaryl and Aryl Alkyl Chalcogenides

2017

Oxidative chalcogenation reaction using molybdenum(V) reagents provides fast access to a wide range of nonsymmetric aryl sulfides and selenides. The established protocol is tolerated by a variety of labile functions, protecting groups, and aromatic heterocycles. In particular, when labile moieties are present, the use of molybdenum(V) reagents provides superior yields compared to other oxidants.

inorganic chemicalschemistry.chemical_classificationmolybdenum pentachloridedisulfides010405 organic chemistryArylOrganic Chemistrychemistry.chemical_elementMolybdenum pentachloride010402 general chemistryoxidative coupling01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryMolybdenumReagentcross-couplingOrganic chemistryOxidative coupling of methaneC–S bond formationAlkylSynlett
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Solid‐state NMR Spectroscopy of Iodine(I) Complexes

2023

Solid-state NMR has been applied to a series of Barluenga-type iodine(I) [L-I-L]PF6 (L=pyridine, 4-ethylpyridine, 4-dimethylaminopyridine, isoquinoline) complexes as their hexafluorophosphate salts, as well as their respective non-liquid ligands (L), their precursor silver(I) complexes, and the respective N-methylated pyridinium and quinolinium hexafluorophoshate salts. These results are compared and contrasted to the corresponding solution studies and single-crystal X-ray structures. As the first study of its kind on the solid-state NMR behavior of halogen(I) complexes, practical considerations are also discussed to encourage wider utilization of this technique in the future. peerReviewed

jodihalogenbondBarluengareagentOrganic Chemistrykiinteän olomuodon kemiaGeneral Chemistrycationexchangeiodine(I)Biochemistrysolid-stateChemistry – An Asian Journal
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