Search results for " Synthesis"

showing 10 items of 1625 documents

Polyhydroxylated indolizidine alkaloids-synthesis of dideoxycastanospermine

2009

The key transformation developed in this work is the anti-Kishi selective dihydroxylation, which proceeds by way of intramolecular participation of the nitrogen protecting group to furnish the desired stereochemistry required for castanospermine like structures. In this paper, we completed a first syn-thesis of a novel dideoxycastanospermine 6. Peer reviewed

Intramolecular reactionStereochemistryOrganic ChemistryIndolizidineBiochemistryChemical synthesischemistry.chemical_compoundCastanosperminechemistryDihydroxylationIntramolecular forceDrug DiscoveryChemical reductionOrganic chemistryProtecting group
researchProduct

Electrochemical characterization of iron sites in ex-framework FeZSM-5

2002

Abstract The electrochemical response of FeZSM-5 prepared by an ex-framework method has been studied using Paraloid B72 polymer film electrodes immersed in aqueous media using H2SO4, HCl, Na2EDTA and NaCl electrolytes. The ex-framework method comprises the hydrothermal synthesis of isomorphously substituted FeZSM-5, followed by calcination at 823 K and subsequent steam treatment (300 mbar H2O in N2) at 873 K. During this process iron is extracted to extra-framework positions. Also partial dealumination of the zeolite framework takes place. Characteristic voltammetric responses in the +1.0 to −0.6 V versus SCE potential range have been recorded and were used to characterize the iron species …

Ion exchangeChemistryGeneral Chemical EngineeringInorganic chemistryIron oxideElectrochemistryAnalytical Chemistrylaw.inventionchemistry.chemical_compoundlawElectrochemistryHydrothermal synthesisCalcinationCyclic voltammetryZeoliteDissolutionJournal of Electroanalytical Chemistry
researchProduct

Ionic liquid crystals based on 3-perfluoalkyl-1,2,4-triazol-4-ium salts

2016

Liquid-crystalline ionic liquids (LC-ILs) are a class of organic materials that of great current interest: they are defined as organic salts that possess the properties of two interesting kinds of material – ionic liquids (ILs) and liquid crystals (LCs). LC-ILs combine many interesting features of ILs (e.g. low volatility and the ability to dissolve solutes with a range of polarities) as well as many attractive properties of LCs (e.g. their intrinsic order and anisotropy). This provides unique opportunities that can be exploited in many different fields, for example their use as solvents for extraction processes as well as electrolytes for batteries, fuel cells, and dye-sensitised solar cel…

Ionic Liquids Fluorinated ionic liquidsIonic liquid crystals Liquid-crystalline ionic liquids Fluorinated ionic liquids crystals Physical and thermal properties Triazolium Synthesis PFCs Crystal structures Smectic Phase.Settore CHIM/06 - Chimica Organica
researchProduct

Ionic Liquids: Media for Better Molecular Catalysis

2004

Ionic liquids (ILs) are more and more suggested as substitutes for traditional solvents in organic synthesis and catalysis. They are suitable candidates for the dissolution of ionic complexes. They can activate and retain them in a polar state: in fact, they act as sequestrands, opening the route to two-phase processes and easier catalyst recovery. This paper reviews authors' results with the development of new syntheses of ILs and applications in carbon–carbon bond formation (dimerisation of methyl acrylate) and redistribution (ring closing metathesis) reactions using ionic precatalysts.

Ionic bondingGeneral MedicineGeneral ChemistryCombinatorial chemistryCatalysisCatalysischemistry.chemical_compoundRing-closing metathesischemistryIonic liquidOrganic chemistryRedistribution (chemistry)Organic synthesisMethyl acrylateDissolutionTopics in Catalysis
researchProduct

The elemental role of iron in DNA synthesis and repair

2017

Iron is an essential redox element that functions as a cofactor in many metabolic pathways. Critical enzymes in DNA metabolism, including multiple DNA repair enzymes (helicases, nucleases, glycosylases, demethylases) and ribonucleotide reductase, use iron as an indispensable cofactor to function. Recent striking results have revealed that the catalytic subunit of DNA polymerases also contains conserved cysteine-rich motifs that bind iron–sulfur (Fe/S) clusters that are essential for the formation of stable and active complexes. In line with this, mitochondrial and cytoplasmic defects in Fe/S cluster biogenesis and insertion into the nuclear iron-requiring enzymes involved in DNA synthesis a…

Iron-Sulfur Proteins0301 basic medicineDNA RepairDNA polymeraseDNA damageDNA repairIronBiophysicsDNA repairEukaryotic DNA replicationSaccharomyces cerevisiaeBiochemistryDNA GlycosylasesBiomaterials03 medical and health sciencesRibonucleotide ReductasesHumansProtein–DNA interactionRibonucleotide reductaseReplication protein Achemistry.chemical_classificationDNA ligaseDeoxyribonucleasesDNA synthesis030102 biochemistry & molecular biologybiologyIron deficiencyDNA HelicasesMetals and AlloysHelicaseDNAYeast030104 developmental biologyIron cofactorBiochemistrychemistryChemistry (miscellaneous)biology.proteinIron-sulfur clusterMetallomics
researchProduct

Organocatalytic Enantioselective Synthesis of Pyrazoles Bearing a Quaternary Stereocenter

2016

An efficient one-pot asymmetric synthesis of pyrazoles bearing a chiral quaternary stereocenter has been developed. Quinine-derived thiourea catalyzed the enantioselective addition of pyrazolones to isatin-derived ketimines, providing the corresponding acetylated pyrazoles after in situ treatment with Ac2O/Et3N. The corresponding pyrazoles were afforded in high yields and excellent enantioselectivities.

Isatin-derived ketimines010402 general chemistry01 natural sciencesBiochemistryCatalysisStereocenterchemistry.chemical_compoundCatàlisiCompostos orgànicsAsymmetric catalysisOrganic chemistryOrganocatalysis010405 organic chemistryChemistryEstereoquímicaOrganic ChemistryEnantioselective synthesisGeneral ChemistryQuaternary stereocenters0104 chemical sciencesThioureaFISICA APLICADAOrganocatalysisPyrazolesPyrazolonesQuímica orgànica
researchProduct

Regulation of Acetylcholine Synthesis and Release in the Isolated Heart

1981

In the two decades following Loewi’s work (8,9) on the frog heart several research groups tried to use the isolated heart preparation from higher vertebrates for further investigations on synthesis, release and inactivation of acetylcholine (ACh). However the results were discouraging because the overflow of ACh during vagal stimulation was near, or below, the limit of the assay.

Isolated Heart PreparationNerve stimulationResearch groupsVagal stimulationAcetylcholine synthesisChemistrymedicineIsolated heartPharmacologyAcetylcholinemedicine.drug
researchProduct

Induction of Cell Differentiation in Transformed Keratinocytes by Synthetic (Glyco)peptides from the Homophilic Recognition Domain of E-Cadherin

2002

KeratinocytesProtein ConformationCadherinChemistryStereochemistryCellular differentiationMolecular Sequence DataGlycopeptidesCell DifferentiationGeneral ChemistryCadherinsPeptide FragmentsCatalysisGlycopeptideProtein Structure TertiaryDomain (software engineering)Cell biologySolid-phase synthesisMicroscopy FluorescenceHumansAmino Acid SequenceNuclear Magnetic Resonance BiomolecularCell Line TransformedAngewandte Chemie International Edition
researchProduct

Synthesis and biological evaluation of dehydroabietic acid derivatives.

2010

A series of C18-oxygenated derivatives of dehydroabietic acid were synthesized from commercial abietic acid and evaluated for their cytotoxic, antimycotic, and antiviral activities.

KetoneAntifungal AgentsCarboxylic acidAntineoplastic AgentsHerpesvirus 1 HumanMicrobial Sensitivity TestsAldehydeChemical synthesisAntiviral Agentschemistry.chemical_compoundInhibitory Concentration 50Cell Line TumorDrug DiscoveryOrganic chemistryAnimalsHumansAbietic acidCytotoxicityPharmacologychemistry.chemical_classificationOrganic ChemistryFungifood and beveragesGeneral Medicineequipment and suppliesTerpenoidchemistryAbietaneslipids (amino acids peptides and proteins)DiterpeneHydrophobic and Hydrophilic InteractionsEuropean journal of medicinal chemistry
researchProduct

Synthesis of novel antimitotic agents based on 2-amino-3-aroyl-5-(hetero)arylethynyl thiophene derivatives

2011

Microtubules are dynamic structures that play a crucial role in cellular division and are recognized as an important target for cancer therapy. In search of new compounds with strong antiproliferative activity and simple molecular structure, a new series of 2-amino-3-(3',4',5'-trimethoxybenzoyl)-5-(hetero)aryl ethynyl thiophene derivatives was prepared by the Sonogashira coupling reaction of the corresponding 5-bromothiophenes with several (hetero)aryl acetylenes. When these compounds were analyzed in vitro for their inhibition of cell proliferation, the 2- and 3-thiophenyl acetylene derivatives were the most powerful compounds, both of which exerted cytostatic effects at submicromolar conc…

KetoneCell divisionStereochemistryClinical BiochemistryPharmaceutical ScienceSonogashira couplingUterine Cervical NeoplasmsEthermacromolecular substancesThiophenesAntimitotic AgentsBiochemistryChemical synthesisArticlechemistry.chemical_compoundMiceStructure-Activity RelationshipThiopheneCell Line TumorDrug DiscoveryThiopheneAnimalsHumansInhibition of tumor cell growthMolecular BiologyCell Proliferationchemistry.chemical_classificationLeukemiaMolecular StructureInhibition of tubulin polymerizationCell growthArylOrganic ChemistryAntiproliferative agentsAntiproliferative agents; Inhibition of tubulin polymerization; Inhibition of tumor cell growth; Thiophene;chemistryMolecular MedicineFemale
researchProduct