Search results for "Chemical synthesi"

showing 10 items of 292 documents

Temperature influence on the synthesis of pristine graphene oxide and graphite oxide

2015

Abstract Derivative oxide carbon materials, such as graphene or graphite oxides, have been recently considered to be a promising material in a wide scenarios of emerging technologies due to their physical and chemical properties, as well as, for their low production costs. Even if apparently similar, these materials exhibit different physical and chemical properties. One of the critical issue is associated with the exfoliation process and contributes to the formation of graphene oxide and graphite oxide material. Here, we show a single synthetic wet method to produce graphene or graphite oxide by applying a control of the operational temperature during the reaction. The process was optimise…

NanostructureMaterials scienceGrapheneMonolayerOxidechemistry.chemical_elementNanotechnologyGraphite oxideCondensed Matter PhysicsChemical synthesiExfoliation jointlaw.inventionchemistry.chemical_compoundchemistrylawMultilayerMonolayerGeneral Materials ScienceMaterials Science (all)GraphiteCarbonGraphene oxide paperMaterials Chemistry and Physics
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Electrochemical deposition of Ag2Se nanostructures

2017

Abstract AgSe based nanostructures (nanowires or nanotubes) were obtained by electrodeposition. A systematic investigation was carried out, varying concentration of the precursors, pH of the electrolytic solution, ligands, and deposition mode, to study the effect of all these parameters on the growth of nanostructures. Nanostructure morphology depends also on the type of metal that was used as support, due to the secondary reaction of hydrogen evolution. On Ni support, the H2 evolution reaction led to formation of only nanotubes, while on copper substrate also nanowires were obtained. Composition of nanostructures depends strongly on solution pH. X-ray diffraction and Raman spectroscopy sho…

NanostructureMaterials scienceNanostructureNanowire02 engineering and technologyElectrolyteCondensed Matter PhysicInorganic compound010402 general chemistryElectrochemistry01 natural sciencesChemical synthesiMetalsymbols.namesakeGeneral Materials ScienceMechanics of MaterialMechanical Engineering021001 nanoscience & nanotechnologyCondensed Matter Physics0104 chemical sciencesX-ray diffractionCrystallographySettore ING-IND/23 - Chimica Fisica ApplicataChemical engineeringMechanics of Materialsvisual_artX-ray crystallographyRaman spectroscopyvisual_art.visual_art_mediumsymbolsOrthorhombic crystal systemMaterials Science (all)0210 nano-technologyRaman spectroscopy
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Selenium and tellurium nanomaterials

2018

Abstract Over the last 40 years, the rapid and exponential growth of nanotechnology led to the development of various synthesis methodologies to generate nanomaterials different in size, shape and composition to be applied in various fields. In particular, nanostructures composed of Selenium (Se) or Tellurium (Te) have attracted increasing interest, due to their intermediate nature between metallic and non-metallic elements, being defined as metalloids. Indeed, this key shared feature of Se and Te allows us the use of their compounds in a variety of applications fields, such as for manufacturing photocells, photographic exposure meters, piezoelectric devices, and thermoelectric materials, t…

NanowireGeneral Physics and AstronomyNanoparticlechemistry.chemical_elementNanotechnology02 engineering and technology010402 general chemistry01 natural sciencesChemical synthesisNanomaterialstelluriumGeneral Materials SciencePhysical synthesisseleniumnanomaterialsGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical scienceschemistrynanowiresphysical synthesisNanorodnanoparticles0210 nano-technologyTelluriumnanorodsselenium tellurium nanomaterials chemical synthesis physical synthesis nanoparticles nanorods nanowiresSeleniumchemical synthesis
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[2+2+2] Cycloadditions of Alkynylynamides - A Total Synthesis of Perlolyrine and the First Total Synthesis of “Isoperlolyrine”

2011

The total syntheses of the carboline alkaloids perlolyrine and "isoperlolyrine" are reported. Key-steps of the syntheses are Negishi coupling reactions on alkynylynamides and their metal-catalyzed [2+2+2] cycloadditions with nitriles to form the β- and γ-carboline cores. The choice of the catalyst strongly affects the β/γ ratio. Spectroscopic features of the γ-isomer are distinctly different from those of the naturally occurring isoperlolyrine.

NitrileChemistryNegishi couplingmedicine.drug_classStereochemistryOrganic ChemistryTotal synthesischemistry.chemical_elementCarboxamideChemical synthesisCycloadditionRhodiumCatalysischemistry.chemical_compoundmedicinePhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Pyrrolo[2,1-d][1,2,3,5]tetrazine-4(3H)-ones, a new class of azolotetrazines with potent antitumor activity.

2003

Pyrrolo[2,1-d][1,2,3,5]tetrazinones 10a-o, compounds that hold the deaza skeleton of the antitumor drug temozolomide, were prepared by reaction of 2-diazopyrroles 9 and isocyanates. Such a synthetic route represents, among those leading to azolotetrazinones reported so far, the only possible one since attempts to cyclize to the title ring system 2-amino-1-carbamoylpyrroles 11 or the mono substituted 2-triazenopyrrole 12 failed. Compounds 10 were screened at the National Cancer Institute (NCI) for their activity against a panel of about 60 human tumor cell lines. Most of them possess remarkable antineoplastic activity having GI(50) values in the low micromolar or sub-micromolar range and rea…

NitrileStereochemistryHL60Clinical BiochemistryPharmaceutical ScienceAntineoplastic AgentsHL-60 CellsBiochemistryChemical synthesischemistry.chemical_compoundTetrazineMiceStructure-Activity RelationshipDrug DiscoverymedicineStructure–activity relationshipAnimalsHumansPyrrolesMolecular BiologyTemozolomideBicyclic moleculeOrganic ChemistryImidazolesMechanism of actionchemistryNitrogen Mustard CompoundsMolecular Medicinemedicine.symptomDrug Screening Assays AntitumorK562 Cellsmedicine.drugIsocyanatesBioorganicmedicinal chemistry
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Synthesis of the new ring system pyrrolizino[2,3-b]indol-4(5H)-one

2011

Derivatives of the new ring system pyrrolizino[2,3-b]indol-4(5H)-one were prepared in four steps starting from substituted benzonitriles bearing a functionalized amino group in the adjacent position. The unsubstituted- and the dimethoxy-pyrrolizinoindolones 5a and 5b exhibited modest activity against the HL-60(TB) human leukemia cell line, whereas the N-methylated dimethoxy-pyrrolizinoindolone 6b showed to be selective against MOLT-4 leukemia, A549/ATCC, HOP-92, and NCI-H460 non-small cell lung cancer, and CAKI-1 renal cancer cell lines.

NitrileStereochemistryOrganic ChemistryCancerBiological activityRing (chemistry)medicine.diseaseSettore CHIM/08 - Chimica FarmaceuticaBiochemistryChemical synthesisPyrrolizino[2; 3-b]indol-4(5H)-one Tripentone Antitumor activity Antitubulin agentsPyrrolizino[23-b]indol-4(5H)-one Tripentone Antitumor activity Antitubulin agentschemistry.chemical_compoundLeukemia3-b]indol-4(5H)-one Tripentone Antitumor activity Antitubulin agentschemistryCell cultureDrug DiscoveryPyrrolizino[2medicineSelectivity
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Triazolopyridines. Part 28. The ring–chain isomerization strategy: triazolopyridine- and triazoloquinoline–pyridine based fluorescence ligands

2012

Abstract The ring–chain isomerization of [1,2,3]triazolo[1,5-a]pyridines or [1,2,3]triazolo[1,5-a] quinolines has been efficiently employed as a tool to provide tridentate fluorescent structures. Based on these scaffolds, a new family of highly fluorescent compounds has been synthesized and evaluated for the recognition of zinc or copper cations. In addition, the 1:1 Zn+2-L complex of a naphthalene triazolopyridine–pyridine derivative revealed high efficiency as sensor for anions providing large binding constants for nitrite and cyanide.

Nitrile[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryLigandStereochemistryCyanideOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistryChemical synthesisCombinatorial chemistry0104 chemical scienceschemistry.chemical_compoundMolecular recognitionchemistryDrug DiscoveryPyridineTriazolopyridineIsomerizationTetrahedron
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Radiosynthesis of 1-(4-(2-[18F]fluoroethoxy)benzenesulfonyl)-3-butyl urea: a potentialβ-cell imaging agent

2002

Summary Tolbutamide (1) is a sulfonurea agent used to stimulate insulin secretion in type 2 diabetic patients. Its analogue 1-(4-(2-[ 18 F]fluoroethoxy)benzenesulfonyl)-3butyl urea (3) was synthesized in overall radiochemical yields of 45% as a potential b-cell imaging agent. Compound 3 was synthesized by 18 F-fluoroalkylation of the corresponding hydroxy precursor (2 )w ith 2-[ 18 F]fluoroethyltosylate in DMF at 1208C for 10 min followed by purification with HPLC in a synthesis time of 50 min. Insulin secretion experiments of the authentic 19 F-standard compound on rat islets showed that the compound has a similar stimulating effect on insulin secretion as that of tolbutamide (1). The part…

OctanolInsulinmedicine.medical_treatmentOrganic ChemistryRadiosynthesisBiochemistryMedicinal chemistryHigh-performance liquid chromatographyChemical synthesisAnalytical ChemistryPartition coefficientchemistry.chemical_compoundTolbutamideBiochemistrychemistryDrug DiscoverymedicineUreaRadiology Nuclear Medicine and imagingSpectroscopymedicine.drugJournal of Labelled Compounds and Radiopharmaceuticals
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Synthesis of 1-Palmitoyl-2-((E)-9- and (E)-10-nitrooleoyl)-sn-glycero-3-phosphatidylcholines

2019

Extensive investigation of nitrated phospholipids in connection with various biologically important processes requires reliable access to suitable material. A selective chemical synthesis introducing a defined nitrofatty acid at the sn-2 position of a 2-lyso sn-glycero-3-phosphatidylcholine was developed. Given that the nitroalkene moiety of both reactant nitrofatty acid derivative and the product esters is characterised by particular sensitivity to nucleophile addition and, depending on the intermediate, subsequent olefin isomerisation and retro-Henry-type reaction, a reliable two-step ester formation was introduced. The activation of the nitrofatty acid succeeded after reaction with trich…

Olefin fiber010405 organic chemistryOrganic Chemistry010402 general chemistryNitroalkene01 natural sciencesChemical synthesisCombinatorial chemistryChlorideCatalysis0104 chemical scienceschemistry.chemical_compoundNucleophilechemistryYield (chemistry)ReagentmedicineMoietylipids (amino acids peptides and proteins)medicine.drugSynthesis
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Improved scalable syntheses of mono- and bis-urethane derivatives of ornithine.

2001

In the search for a practical route to ornithine bisurethane derivatives useful for peptide synthesis, we elaborated the simple and efficient (86% yield) synthesis of N(epsilon)-tert-butoxycarbonyl-L-ornithine copper(II) complex (1). This served as substrate for obtaining N(epsilon)-tert-butoxycarbonyl-L-ornithine (2), N(alpha)-benzyloxycarbonyl-N(epsilon)-tert-butoxycarbonyl-L-ornithine (3) and N(alpha)-(9-fluorenyl)methoxycarbonyl-N(epsilon)-tert-butoxycarbonyl-L-ornithine (4). These were synthesized in 94-95% yields and with a purity above 99%.

OrnithineCalorimetry Differential ScanningChemistrychemistry.chemical_elementSubstrate (chemistry)General ChemistryGeneral MedicineOrnithineChemical synthesisCopperUrethanechemistry.chemical_compoundYield (chemistry)One pot reactionDrug DiscoveryPeptide synthesisOrganic chemistryIndicators and ReagentsProtecting groupChromatography High Pressure LiquidCopperChemicalpharmaceutical bulletin
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