Search results for "Organic Synthesis"

showing 10 items of 82 documents

PREPARATION AND CHARACTERIZATION OF BROOKITE TiO2 PHOTOCATALYSTS FOR POLLUTANTS DEGRADATION AND ORGANIC SYNTHESIS

2012

Brookite TiO2 phoocatalysis organic synthesisSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie
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MoVReagents in Organic Synthesis (Eur. J. Org. Chem. 11/2016)

2016

C c couplingchemistry.chemical_compoundchemistryMolybdenumReagentOrganic Chemistrychemistry.chemical_elementOrganic chemistryOxidative coupling of methaneOrganic synthesisPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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An expeditious synthesis of spinasterol and schottenol, two phytosterols present in argan oil and in cactus pear seed oil, and evaluation of their bi…

2015

International audience; Spinasterol and schottenol, two phytosterols present in argan oil and in cactus pear seed oil, were synthesized from commercially available stigmasterol by a four steps reactions. In addition, the effects of these phytosterols on cell growth and mitochondrial activity were evaluated on 158N murine oligodendrocytes, C6 rat glioma cells, and SK-N-BE human neuronal cells with the crystal violet test and the MTT test, respectively. The effects of spinasterol and schottenol were compared with 7-ketocholesterol (71CC) and ferulic acid, which is also present in argan and cactus pear seed oil. Whatever the cells considered, dose dependent cytotoxic effects of 71CC were obser…

Central Nervous Systemfood.ingredientCrystal violet testClinical BiochemistryStigmasterol[ PHYS.COND.CM-MS ] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Argan oilOrganic synthesisBiologyBiochemistryCell LineFerulic acidPyruschemistry.chemical_compoundMiceEndocrinologyfoodSchottenolCytotoxic T cellAnimalsHumansPlant OilsMolecular BiologySpinasterolCell ProliferationPharmacologyPEARMIT testStigmasterolCell growthOrganic ChemistryPhytosterolsNervous cellsSitosterolsMitochondriaRatsSpinasterolchemistryBiochemistryCactusSeeds
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Electro-organic Synthesis as a Sustainable Alternative for Dehydrogenative Cross-Coupling of Phenols and Naphthols

2016

The dehydrogenative cross-coupling of phenols and naphthols can be achieved by several oxidative methods. However, the key is the use of fluorinated alcohols such as 1,1,1,3,3,3-hexafluoroisopropanol. The direct application of electricity represents an alternative synthetic approach, which is superior to other oxidizers (e.g., peroxides). The method is sustainable, inherently safe, and easily scalable.

Chemical substance010405 organic chemistryChemistryAnodic oxidationOrganic Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundCoupling (computer programming)Organic chemistryOrganic synthesisPhenolsSynthesis
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Organic synthesis of high added value molecules with MOF catalysts

2020

Recent examples of organic synthesis of fine chemicals and pharmaceuticals in confined spaces of MOFs are highlighted and compared with silica-based ordered porous solids, such as zeolites or mesoporous (organo)silica. These heterogeneous catalysts offer the possibility of stabilizing the desired transition states and/or intermediates during organic transformations of functional groups and (C-C/C-N) bond forming steps towards the desired functional high added value molecular scaffolds. A short introduction on zeolites, mesoporous silica and metal-organic frameworks is followed by relevant applications in which confined active sites in the pores promote single or multi-step organic synthesis…

Chemistry OrganicBiochemistryCatalysischemistry.chemical_compoundLEVULINIC ACIDALLYLIC ALCOHOLSMoleculePhysical and Theoretical ChemistryConfined spaceScience & TechnologyChemistryOrganic ChemistryMesoporous silicaMISSING-LINKER DEFECTSTransition stateMESOPOROUS MATERIALSChemistryRECYCLABLE CATALYSTChemical engineeringHETEROGENEOUS CATALYSISC-CMETALPhysical SciencesACTIVE-SITESOrganic synthesisPorous solidsMesoporous materialPROSTAGLANDIN UNSATURATED-KETONESOrganic & Biomolecular Chemistry
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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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Method development for the determination of 1,1-dimethylhydrazine by the high-performance liquid chromatography-mass spectrometry technique.

2018

Unsymmetrical dimethyl hydrazine is highly toxic, carcinogenic compound, widely used for organic synthesis and drug development. Therefore, due to its high reactivity, direct analysis is problematic. Current study proposes to use derivatization reaction to increase selectivity and sensitivity of high-performance liquid chromatography–mass spectrometry method. Different derivatization agents were tested and optimal reaction media was found. Derivatization was performed by using small amounts of reagents to lower the cost of analysis. The full validation of the method was performed and it can be used in a routine control in pharmaceutical analysis. Method sensitivity is 0.15 ppm, and lineari…

ChromatographyElectrospray ionization010401 analytical chemistryGeneral Medicine010402 general chemistryTandem mass spectrometryMass spectrometry01 natural sciencesHigh-performance liquid chromatographyAtomic and Molecular Physics and Optics0104 chemical scienceschemistry.chemical_compoundchemistryDimethylhydrazineReactivity (chemistry)Organic synthesisDerivatizationSpectroscopyEuropean journal of mass spectrometry (Chichester, England)
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Evaluation of Cyclic Amides as Activating Groups in N-C Bond Cross-Coupling: Discovery of N-Acyl-δ-valerolactams as Effective Twisted Amide Precursor…

2021

The development of efficient methods for facilitating N-C(O) bond activation in amides is an important objective in organic synthesis that permits the manipulation of the traditionally unreactive amide bonds. Herein, we report a comparative evaluation of a series of cyclic amides as activating groups in amide N-C(O) bond cross-coupling. Evaluation of N-acyl-imides, N-acyl-lactams, and N-acyl-oxazolidinones bearing five- and six-membered rings using Pd(II)-NHC and Pd-phosphine systems reveals the relative reactivity order of N-activating groups in Suzuki-Miyaura cross-coupling. The reactivity of activated phenolic esters and thioesters is evaluated for comparison in O-C(O) and S-C(O) cross-c…

Coupling (electronics)chemistry.chemical_compoundChemistryStereochemistryAmideOrganic ChemistryElectrophilePeptide bondReactivity (chemistry)Organic synthesisResonance (chemistry)Coupling reactionJournal of Organic Chemistry
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Organotitanium reagents in organic synthesis a simple means to adjust reactivity and selectivity of carbanions

1982

Cyclic ketonechemistry.chemical_compoundchemistryReagentOrganic chemistryOrganic synthesisReactivity (chemistry)SelectivityAsymmetric inductionCarbanion
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Urīnskābes reakcija ar etiķskābes anhidrīdu: diplomdarbs

1937

DiplomdarbiUrīnskābe:NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesis [Research Subject Categories]Ķīmiskās reakcijasAcetic acidUric acidEtiķskābe
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