Search results for " Synthesis"

showing 10 items of 1625 documents

Hydrothermal synthesis of zeolites from rhyolitic pumice of different geological origins

1983

Abstract Twelve samples of rhyolitic pumice from widely different origins were subjected to zeolitization in standard hydrothermal conditions (solid/liquid ratio, 1 5 ; T , 95°C; reaction time, 5 h; alkaline solution 5 N NaOH). The Si Al ratio of the starting material was of special importance in that zeolites formed with Si Al ratios similar to or smaller than that of the parent material. Pumice with low SiO 2 Al 2 O 3 , and high Fe content, preferentially gave rise to zeolites with lower SiO 2 Al 2 O 3 ratio than in the case of lower Fe and higher SiO 2 Al 2 O 3 ratio.

Liquid ratioMaterials sciencegenetic structuresMechanical EngineeringMineralogyFe contentCondensed Matter PhysicsHydrothermal circulationChemical engineeringMechanics of MaterialsPumiceRhyoliteHydrothermal synthesisGeneral Materials Science
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Enantioselective α-alkylation of unsaturated carboxylic acids using a chiral lithium amide

2001

Abstract The regio- and stereochemistry of the alkylation of dienediolates from unsaturated carboxylic acids with benzylic halides, which often results in mixtures of isomers, can be controlled by means of changes in the lithium amide, allowing the α-regioisomer to be obtained as the major diastereoisomer. In addition, when chiral amines are used, moderate enantiomeric excesses can be attained.

Lithium amideChemistryorganic chemicalsfungiOrganic ChemistryEnantioselective synthesisDiastereomerfood and beveragesHalideAlkylationCatalysisInorganic Chemistrychemistry.chemical_compoundpolycyclic compoundsOrganic chemistryheterocyclic compoundsPhysical and Theoretical ChemistryEnantiomerTetrahedron: Asymmetry
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ChemInform Abstract: Enantioselective α-Alkylation of Unsaturated Carboxylic Acids Using a Chiral Lithium Amide.

2010

Abstract The regio- and stereochemistry of the alkylation of dienediolates from unsaturated carboxylic acids with benzylic halides, which often results in mixtures of isomers, can be controlled by means of changes in the lithium amide, allowing the α-regioisomer to be obtained as the major diastereoisomer. In addition, when chiral amines are used, moderate enantiomeric excesses can be attained.

Lithium amideorganic chemicalsfungiDiastereomerEnantioselective synthesisfood and beveragesHalideGeneral MedicineAlkylationchemistry.chemical_compoundchemistrypolycyclic compoundsOrganic chemistryheterocyclic compoundsEnantiomerChemInform
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Gallium Concentration Optimisation of Gallium Doped Zinc Oxide for Improvement of Optical Properties

2021

The research has been supported by project ERA.NET RUS_ST2017-05 (Latvia) and No. 18-52-76002 (Russia). The Institute of Solid State Physics, University of Latvia as the Centre of Excellence has received funding from the European Union’s Hori-zon 2020 Framework Programme H2020-WIDESPREAD-01-2016-2017-Teaming-Phase2 under grant agreement No. 739508, project CAMART².

Luminescencezno:gaQC1-999Inorganic chemistryGeneral Physics and Astronomychemistry.chemical_element02 engineering and technologyZincScintillator010402 general chemistry01 natural sciencesoptimised concentration:NATURAL SCIENCES:Physics [Research Subject Categories]luminescenceGalliumPhysicsDopingGeneral EngineeringGa [ZnO]021001 nanoscience & nanotechnology0104 chemical sciencesscintillatorchemistrymicrowave-assisted solvothermal synthesis0210 nano-technologyLuminescenceLatvian Journal of Physics and Technical Sciences
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Metabolic fluxes and l-lysine synthesis by Corynebacterium glutamicum in relation to cellular total reducing activity

2001

Abstract The total reducing activity (TRA) of cells was used to estimate the physiological activity of Corynebacterium glutamicum under conditions of l -lysine synthesis. This was estimated as the rate of reduction of 2,3,5- triphenyltetrazolium chloride by intact cells. TRA of cells was linearly correlated with the intracellular concentrations of RNA and the bacterial growth rate. It was concluded that this activity reflected the rate of energy generation in cells. A decrease in TRA of growing cells was related to an increase in bacterial lysine synthesis activity. Alteration in metabolic pathway functioning and an increase in the intracellular concentrations of lysine precursors favoured …

LysineRNABioengineeringBacterial growthBiologycomplex mixturesApplied Microbiology and BiotechnologyBiochemistryCorynebacterium glutamicumMetabolic pathwayBiochemistrybacteriaLysine synthesisreproductive and urinary physiologyIntracellularTriphenyltetrazolium chlorideProcess Biochemistry
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Coordination networks incorporating halogen-bond donor sites and azobenzene groups

2016

Two Zn coordination networks, {[Zn(1)(Py)2]2(2-propanol)}n (3) and {[Zn(1)2(Bipy)2](DMF)2}n (4), incorporating halogen-bond (XB) donor sites and azobenzene groups have been synthesized and fully characterized. Obtaining 3 and 4 confirms that it is possible to use a ligand wherein its coordination bond acceptor sites and XB donor sites are on the same molecular scaffold (i.e., an aromatic ring) without interfering with each other. We demonstrate that XBs play a fundamental role in the architectures and properties of the obtained coordination networks. In 3, XBs promote the formation of 2D supramolecular layers, which, by overlapping each other, allow the incorporation of 2-propanol as a gues…

MOF Supramolecular Chemistry Halogen Bonding AzobenzeneStereochemistry116 Chemical sciencesSupramolecular chemistry02 engineering and technology010402 general chemistryRing (chemistry)01 natural sciencesIUPAC RECOMMENDATIONS 2013chemistry.chemical_compoundMETAL-ORGANIC FRAMEWORKSdell'Università e della RicercaCHEMISTRYTO-CRYSTAL ISOMERIZATIONMinistero dell'IstruzioneMoleculeGeneral Materials Scienceta215SUPRAMOLECULAR SYNTHESISHalogen bondMETAL-ORGANIC FRAMEWORKS; IUPAC RECOMMENDATIONS 2013; TO-CRYSTAL ISOMERIZATION; SUPRAMOLECULAR SYNTHESIS; VISIBLE-LIGHT; POLYMERS; FLUOROAZOBENZENES; COCRYSTALS; COMPLEXES; CHEMISTRYLigandChemistryFLUOROAZOBENZENESMinistero dell'Istruzione dell'Università e della RicercaGeneral ChemistryCOCRYSTALS021001 nanoscience & nanotechnologyCondensed Matter PhysicsAcceptor0104 chemical sciencesCrystallographyAzobenzeneMIURMetal-organic frameworkCOMPLEXESSettore CHIM/07 - Fondamenti Chimici Delle TecnologieVISIBLE-LIGHTPOLYMERS0210 nano-technology
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Total synthesis of two potent anti-inflammatory macrolactones of the oxacyclododecindione type

2015

An esterification/Friedel-Crafts-cyclization approach permitted the first successful synthetic entry into the oxacyclododecindione subclass of the dihydroxyphenylacetic acid lactone-type natural products. This route allowed the preparation of two highly active anti-inflammatory fungal secondary metabolites 14-deoxyoxacyclododecindione and 14-deoxy-4-dechlorooxacyclododecindione as well as their 14-desmethyl analogues.

Macrocyclic CompoundsMolecular StructureChemistrymedicine.drug_classDihydroxyphenylacetic acidStereochemistryAnti-Inflammatory Agents Non-SteroidalOrganic ChemistryTotal synthesisBiochemistrySubclassAnti-inflammatoryLactonesBiochemistryCyclizationmedicineOxacyclododecindionePhysical and Theoretical ChemistryOrganic & Biomolecular Chemistry
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Total synthesis and biological evaluation of seven new anti-inflammatory oxacyclododecindione-type macrolactones

2020

Through variation of our previously published total synthesis of two highly active anti-inflammatory macrolactones from the oxacyclododecindione family (J. Tauber, M. Rohr, T. Walter, G. Erkel and T. Opatz, Org. Biomol. Chem., 2015, 13, 7813-7821), seven new representatives of this compound class were prepared. Substitution of the 14-hydroxy group in oxacyclododecindione with a methyl substituent provided a readily accessible non-natural analogue which has similar pharmacological properties to the scarcely available natural product. Since the producible amount of substance is therefore no longer restricted by low fermentation yields, extensive in vivo studies become possible for the first t…

Macrocyclic CompoundsNatural productStereochemistryOrganic ChemistrySubstituentTotal synthesisBiochemistrychemistry.chemical_compoundchemistryIn vivoSide chainBioassayFermentationPhysical and Theoretical ChemistryIC50Organic & Biomolecular Chemistry
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Synthesis of Lamellarin U and Lamellarin G Trimethyl Ether by Alkylation of a Deprotonated α-Aminonitrile

2008

1,2,3,4-Tetrahydroisoquinoline-1-carbonitriles can serve as starting materials for the one-pot synthesis of 5,6-dihydropyrrolo[2,1 a]isoquinolines and 1-benzyl-3,4-dihydroisoquinolines. The latter compounds were transformed to lamellarin G trimethyl ether and lamellarin U in short reaction sequences. This method allows the introduction of acid-sensitive protecting groups for the phenolic hydroxy functions which would be cleaved under the harsh conditions of the classical Bischler-Napieralski reaction.

Magnetic Resonance SpectroscopyAlkylationSpectrophotometry InfraredNitrileStereochemistryOrganic ChemistryEtherNuclear magnetic resonance spectroscopyAlkylationIsoquinolinesHeterocyclic Compounds 4 or More RingsChemical synthesisMass Spectrometrychemistry.chemical_compoundDeprotonationchemistryCoumarinsNitrilesProtecting groupBischler–Napieralski reactionThe Journal of Organic Chemistry
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1-Pyrrolines (3,4-Dihydro-2H-pyrroles) as a Template for New Drugs

2001

Magnetic Resonance SpectroscopyChemistryDrug DesignDrug DiscoveryPharmaceutical ScienceOrganic chemistryIndicators and ReagentsPyrrolesStereoisomerismCombinatorial chemistryChemical synthesisPyrrole derivativesAntibacterial agentArchiv der Pharmazie
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