Search results for "lcsh:QD241-441"

showing 10 items of 438 documents

Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents

2020

Aryl benzoates are compounds of high importance in organic synthesis. Herein, we report the iron-catalyzed C(sp2)&ndash

Chlorobenzoatesaryl estersPharmaceutical ScienceMedicinal chemistryArticleCatalysisAnalytical ChemistryCatalysislcsh:QD241-441chemistry.chemical_compoundironlcsh:Organic chemistryDrug Discoverycross-couplingPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationNucleophilic additionMolecular StructureArylOrganic ChemistryBenzoatesChlorobenzoateschemistryChemistry (miscellaneous)Fe-catalysisFunctional groupKumada cross-couplingMolecular MedicineOrganic synthesisC–O activationIron CompoundsMolecules
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Chemical Composition and Antimicrobial Activity of the Essential Oils from Three Chemotypes of Origanum vulgare L. ssp. hirtum (Link) Ietswaart Growi…

2009

Essential oils obtained from inflorescences of three Origanum vulgare L.ssp. hirtum (Link) Ietswaart samples, growing wild in different locations in Campania (Southern Italy), were analysed. Three chemotypes were found: the first, with a prevalence of carvacrol/thymol; the second, characterized by the prevalence of thymol/alpha-terpineol; the third, featuring a prevalence of linalyl acetate and linalool. This chemical study attempts to provide a contribution in shedding light on the relationship between chemical composition and biotypes and/or chemotypes in Origanum vulgare ssp. hirtum. The essential oils were also evaluated for their antibacterial activity against 10 selected microorganism…

Chromatography GasAcyclic MonoterpenescarvacrolPharmaceutical ScienceCyclohexane MonoterpenesMicrobial Sensitivity TestsLinalyl acetateCymenesArticleGas Chromatography-Mass SpectrometryAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundOriganum vulgare ssp. hirtumantibacterial activitylcsh:Organic chemistryLinaloolOriganumthymolCyclohexenesDrug DiscoveryBotanyOils VolatilePlant OilsCarvacrollinalyl acetatePhysical and Theoretical ChemistryThymolessential oil compositionBacteriabiologyChemotypeOrganic ChemistryOriganum vulgare ssp. hirtum; essential oil composition; thymol; carvacrol; linalyl acetate; antibacterial activityOriganumbiology.organism_classificationAntimicrobialAnti-Bacterial AgentsItalychemistryChemistry (miscellaneous)MonoterpenesCymenesMolecular MedicineMolecules
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Chemical composition and phytotoxic effects of essential oils of Salvia hierosolymitana Boiss. and Salvia multicaulis Vahl. var. simplicifolia Boiss.…

2009

The chemical composition of the essential oils of S. hierosolymitana Boiss. and S. multicaulis Vahl. var. simplicifolia Boiss. collected in Lebanon was studied by means of GC and GC-MS analysis. In all 115 compounds were identified: 82 for S hierosolymitana and 72 for S. multicaulis var. simplicifolia. The presence of carbonylic compounds (17%) characterizes the oil from S. hierosolymitana, while S. multicaulis var. simplicifolia oil is rich of monoterpenes (34.5%) and sesquiterpenes (46.9%). The effects of the essential oils on germination and initial radical elongation of Raphanus sativus L. (radish) and Lepidium sativum L. (garden cress) were studied, indicating in a different activity a…

Chromatography GasPharmaceutical ScienceRaphanusBiologyLepidiumSalvia hierosolymitanaArticleGas Chromatography-Mass Spectrometryessential oilAnalytical Chemistrylaw.inventionRaphanuslcsh:QD241-441Salvia hierosolymitana Boiss.lcsh:Organic chemistrylawDrug DiscoveryBotanyRadicleOils VolatilePlant OilsSalviaPhysical and Theoretical ChemistryLebanonEssential oilOrganic Chemistry<i>Salvia hierosolymitana </i>Boiss.; <i>Salvia multicaulis </i>Vahl. var. <i>simplicifolia </i>Boiss.; essential oil; germination; radical elongationbiology.organism_classificationLepidium sativumradical elongationgerminationChemistry (miscellaneous)GerminationSalvia multicaulis Vahl. var. simplicifolia Boiss.Molecular MedicinePhytotoxicitySalvia multicaulis
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Pauson-Khand reaction of internal dissymmetric trifluoromethyl alkynes. Influence of the alkene on the regioselectivity.

2014

Abstract: The scope of the Pauson-Khand reaction (PKR) of internal trifluoromethyl alkynes, previously described with norbornadiene, is expanded to norbornene and ethylene. A thorough structural analysis of the resulting PK adducts has been carried out to unveil that α-trifluoromethylcyclopentenones are preferred in all cases, independently of the electronic properties of the alkyne. The regioselectivity observed with norbornadiene and ethylene is higher than in the case of norbornene.

Ciclització (Química)EthyleneHydrocarbons FluorinatedStereochemistryNorbornadieneQuímica organometàl·licaPharmaceutical ScienceAlkynetrifluoromethylalkynesCrystallography X-RayArticlecyclopentenonesAnalytical ChemistryRing formation (Chemistry)cycloadditionslcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryDrug DiscoveryPhysical and Theoretical ChemistryNorbornenechemistry.chemical_classificationPauson-Khand reactionTrifluoromethylMolecular StructureAlkenePauson–Khand reactionOrganic ChemistryRegioselectivityStereoisomerismCobaltEthylenesNorbornaneschemistryOrganometallic chemistryChemistry (miscellaneous)AlkynesregioselectivityMolecular MedicineMolecules (Basel, Switzerland)
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Supramolecular polymerization of sulfated dendritic peptide amphiphiles into multivalent L-selectin binders

2021

The synthesis of a sulfate-modified dendritic peptide amphiphile and its self-assembly into one-dimensional rod-like architectures in aqueous medium is reported. The influence of the ionic strength on the supramolecular polymerization was probed via circular dichroism spectroscopy and cryogenic transmission electron microscopy. Physiological salt concentrations efficiently screen the charges of the dendritic building block equipped with eight sulfate groups and trigger the formation of rigid supramolecular polymers. Since multivalent sulfated supramolecular structures mimic naturally occurring L-selectin ligands, the corresponding affinity was evaluated using a competitive SPR binding assay…

Circular dichroismSupramolecular chemistryPeptidemacromolecular substancesFull Research Paperlcsh:QD241-441lcsh:Organic chemistryAmphiphilePeptide amphiphilelcsh:Sciencel-selectin binderssupramolecular polymerschemistry.chemical_classificationOrganic Chemistrytechnology industry and agriculture547multivalencyCombinatorial chemistryself-assembly in waterSupramolecular polymersChemistry500 Naturwissenschaften und Mathematik::540 Chemie::547 Organische ChemiechemistryPolymerizationIonic strengthlcsh:QBeilstein Journal of Organic Chemistry
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Innovative “Green” and Novel Strategies for the Extraction of Bioactive Added Value Compounds from Citrus Wastes—A Review

2017

Citrus is a major processed crop that results in large quantities of wastes and by-products rich in various bioactive compounds such as pectins, water soluble and insoluble antioxidants and essential oils. While some of those wastes are currently valorised by various technologies (yet most are discarded or used for feed), effective, non-toxic and profitable extraction strategies could further significantly promote the valorisation and provide both increased profits and high quality bioactives. The present review will describe and summarize the latest works concerning novel and greener methods for valorisation of citrus by-products. The outcomes and effectiveness of those technologies such a…

CitrusPharmaceutical Sciencecitrus wastes ; ultrasound ; pulsed electric fields ; microwaves ; high pressure ; supercritical CO2ReviewGarbageCitrus wastes; High pressure; Microwaves; Pulsed electric fields; Supercritical CO2; Ultrasound; Citrus; Fruit; Garbage; Green Chemistry Technology; Plant Extracts; Waste Products; Organic ChemistrymicrowavesLower energysupercritical CO2Analytical Chemistrylcsh:QD241-4410404 agricultural biotechnologylcsh:Organic chemistryDrug DiscoveryAdded valuePhysical and Theoretical ChemistryConventional techniqueWaste Products2. Zero hungercitrus wastesPlant Extractsultrasoundbusiness.industryOrganic ChemistryExtraction (chemistry)food and beveragesGreen Chemistry Technology04 agricultural and veterinary sciences040401 food scienceBiotechnologyhigh pressureWater solublepulsed electric fieldsChemistry (miscellaneous)FruitHigh pressureMolecular MedicineEnvironmental scienceBiochemical engineeringValorisationbusinessMolecules
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Volatile Compounds of Lemon and Grapefruit IntegroPectin

2020

An HS-SPME GC-MS analysis of the volatile compounds adsorbed at the outer surface of lemon and grapefruit pectins obtained via the hydrodynamic cavitation of industrial waste streams of lemon and grapefruit peels in water suggests important new findings en route to understanding the powerful and broad biological activity of these new pectic materials. In agreement with the ultralow degree of esterification of these pectins, the high amount of highly bioactive &alpha

Citrusfood.ingredientPectinlemonPhytochemicalsPharmaceutical SciencegrapefruitArticleIndustrial wasteGas Chromatography-Mass SpectrometryAnalytical Chemistrylcsh:QD241-441chemistry.chemical_compoundAdsorptionfoodLinaloolCitrus paradisilcsh:Organic chemistryDrug Discoveryhydrodynamic cavitation?-terpineolFood sciencePhysical and Theoretical ChemistryIntegroPectinpectinResidue (complex analysis)LimoneneVolatile Organic CompoundsMolecular Structureapplied_chemistryOrganic Chemistrycircular economywaste citrus peelBiosynthetic PathwaysTerpineolchemistryChemistry (miscellaneous)FruitMolecular Medicineα-terpineolGas chromatography–mass spectrometryCitric acidCitrus paradisi
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New Anti-Neoplastics Obtained by a Molecular Connectivity Method

2000

Molecular Connectivity is a method, which allows to discriminate different pharmacological activities on the basics of numeric parameters of the molecules in study, related with specific and exclusive indexes. In the present study, we propose two potentially anti-neoplasic compounds: tricromil and zomepirac, by analyzing more than a hundred different chemicals.

Computer scienceOrganic ChemistryPharmaceutical ScienceNanotechnologyComputational biologyAnalytical Chemistrylcsh:QD241-441n/alcsh:Organic chemistryChemistry (miscellaneous)Drug DiscoveryZomepiracmedicineMolecular MedicinePhysical and Theoretical Chemistrymedicine.drugMolecules
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Sample Preparation to Determine Pharmaceutical and Personal Care Products in an All-Water Matrix: Solid Phase Extraction

2020

© 2020 by the authors.

ConcentrationWater samplesPharmaceuticals and personal care productsPharmaceutical ScienceSewageReviewCosmeticsWastewater010501 environmental sciences01 natural sciencesEnvironmental impact of pharmaceuticals and personal care productsAnalytical ChemistryAigua AnàlisiTandem Mass SpectrometryDrug DiscoverySample preparationOnlineSolid phase extractionProcess engineeringGroundwaterChromatography High Pressure LiquidSewageDispersive liquid-liquid microextractionSolid Phase ExtractionDisksPharmaceutical PreparationsWastewaterChemistry (miscellaneous)Molecular MedicineEnvironmental MonitoringFarmacologiaLiquid Phase MicroextractionCartridgesSensitivity and SpecificityWater PurificationIsolationlcsh:QD241-441lcsh:Organic chemistryPhysical and Theoretical Chemistry0105 earth and related environmental sciencesSolid-phase extractionbusiness.industry010401 analytical chemistryOrganic ChemistryAnalytical techniqueExtraction (chemistry)Water0104 chemical sciencesEnvironmental sciencebusinessSurface waterWater Pollutants Chemical
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A conformationally adaptive macrocycle : conformational complexity and host–guest chemistry of zorb[4]arene

2018

Large amplitude conformational change is one of the features of biomolecular recognition and is also the basis for allosteric effects and signal transduction in functional biological systems. However, synthetic receptors with controllable conformational changes are rare. In this article, we present a thorough study on the host–guest chemistry of a conformationally adaptive macrocycle, namely per-O-ethoxyzorb[4]arene (ZB4). Similar to per-O-ethoxyoxatub[4]arene, ZB4 is capable of accommodating a wide range of organic cations. However, ZB4 does not show large amplitude conformational responses to the electronic substituents on the guests. Instead of a linear free-energy relationship, ZB4 foll…

Conformational changeAllosteric regulationSupramolecular chemistryCrystal structure010402 general chemistry01 natural sciencesHeat capacityFull Research Papersupramolecular chemistrylcsh:QD241-441lcsh:Organic chemistryComputational chemistrysupramolekulaarinen kemiahost-guest chemistryhost–guest chemistrylcsh:ScienceHost–guest chemistryta116010405 organic chemistryChemistryComponent (thermodynamics)Hydrogen bondOrganic Chemistryzorb[4]arene0104 chemical sciencesChemistrymacrocyclesconformationslcsh:QBeilstein Journal of Organic Chemistry
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