Search results for "One pot"

showing 10 items of 15 documents

Synthesis of 2-Aminothiazole Derivatives in Easy Two-Step, One-Pot Reaction

2018

010405 organic chemistryChemistryOne pot reactionOrganic ChemistryTwo step2-aminothiazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesJournal of Heterocyclic Chemistry
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Synthesis of Multisubstituted 1,4-Dihydrobenzoxazin-2-ones through a One-Pot Nucleophilic N-Alkylation/C-Alkylation of Cyclic α-Imino Esters

2017

A nucleophilic N-alkylation of 2-oxobenzoxazine-2-carboxylates with organozinc reagents with good selectivities and in moderate to good yields is described. Moreover, the synthesis of multisubstituted 1,4-dihydrobenzoxazine-2-ones bearing a tetrasubstituted carbon atom via a one-pot N-alkylation/C-alkylation reactions is reported.

Carbon atom010405 organic chemistryChemistryOrganic Chemistrychemistry.chemical_elementZincAlkylation010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesUmpolungReaccions químiquesCompostos orgànics SíntesiNucleophileOne pot reactionReagentOrganic chemistrylipids (amino acids peptides and proteins)Química orgànica
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Eine einfache Synthese für N-[3-[3-(1-Piperidinylmethyl)-phenoxy]propyl]hydrazincarbothioamid

1985

Synthese par reaction one pot de l'amino-3″ propoxy-3' benzyl-1 piperidine avec CS 2 , l'iodomethane et l'hydrazine

Carbon disulfidechemistry.chemical_compoundchemistryOne pot reactionDrug DiscoveryPharmaceutical ScienceAliphatic compoundMedicinal chemistryArchiv der Pharmazie
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CoIILnIII dinuclear complexes (LnIII = Gd, Tb, Dy, Ho and Er) as platforms for 1,5-dicyanamide-bridged tetranuclear CoII2LnIII2 complexes: A magneto-…

2012

Five acetate-diphenoxo triply-bridged Co-II-Ln(III) complexes (Ln(I) = Gd, Tb, Dy, Ho, Er) of formula [Co(mu-L)(mu-Ac)Ln(NO3)(2)] and two diphenoxo doubly-bridged Co-II-Ln(III) complexes (Ln(III) = Gd, Tb) of formula [Co(H2O)(mu-L)Ln(NO3)(3)]center dot S (S = H2O or MeOH), were prepared in one pot reaction from the compartmental ligand N,N',N ''-trimethyl-N,N ''-bis(2-hydroxy3-methoxy-5-methylbenzyl)diethylene triamine (H2L). The diphenoxo doubly-bridged Co-II-Ln(III) complexes were used as platforms to obtain 1,5-dicyanamide-bridged tetranuclear Co-II-Ln(III) complexes (Ln(III) = Gd, Tb, Dy, Ho, Er). All exhibit ferromagnetic interactions between the Co-II and Ln(III) ions and in the case …

Chemistry(all)LigandGeneral Chemical EngineeringRelaxation (NMR)MineralogyGeneral ChemistryDiethylene triamineIonchemistry.chemical_compoundMagnetizationCrystallography/dk/atira/pure/subjectarea/asjc/1500chemistryFerromagnetismOne pot reactionChemical Engineering(all)/dk/atira/pure/subjectarea/asjc/1600Dicyanamideta116Comptes Rendus Chimie
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Synthesis of 5-substituted 2,3-dihydrobenzofurans in a one-pot oxidation/cyclization reaction

2011

Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot oxidation/cyclization procedure between para-aminophenol derivatives and an azadiene. Variously substituted 2,3-dihydrobenzofurans have been synthesized according to a sequential one-pot oxidation/cyclization procedure between para-aminophenol derivatives and an azadiene. © 2011 Elsevier Ltd. All rights reserved.

ChemistryOne pot reactionOrganic ChemistryDrug DiscoveryOrganic chemistryOne-pot reaction 23-Dihydrobenzofuran Quinone imide Oxidation CycloadditionSettore CHIM/08 - Chimica FarmaceuticaBiochemistryCycloadditionTetrahedron
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Green and Direct Synthesis of Benzaldehyde and Benzyl Benzoate in One Pot

2018

High yields of valued benzaldehyde and benzyl benzoate are obtained in one pot starting from benzyl alcohol using oxygen as only oxidant under mild conditions (2 bar O2, 100 °C) along with an ultralow amount (0.02 mol %) of Au nanoparticles heterogenized over a spherical ORMOSIL mesoporous support. The process is remarkably selective and the catalyst is stable.

General Chemical EngineeringBenzyl benzoateORMOSILchemistry.chemical_elementGold catalysis010402 general chemistry01 natural sciencesOrmosilOxygenMedicinal chemistryBenzaldehydechemistry.chemical_compoundBenzyl benzoateEnvironmental ChemistryOne pot010405 organic chemistryRenewable Energy Sustainability and the EnvironmentSolagel catalysisGeneral ChemistrySettore CHIM/06 - Chimica OrganicaBenzaldehyde0104 chemical scienceschemistryBenzyl alcoholAerobic oxidationSolâgel catalysis
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Le istituzioni della regolazione

2008

La regolazione non si limita alla sola creazione di regole, ma comprende anche le attività che le rendono più o meno efficaci. Tra le istituzioni della regolazione pubblica andrebbero inclusi, se e in quanto producono regole, non solo i parlamenti (o in genere le assemblee legislative, ricordando peraltro che nel nostro paese divengono sempre più importanti quelle regionali) e gli esecutivi, non solo le istituzioni comunitarie e alcune istituzioni sopranazionali, ma anche i soggetti che hanno il compito di interpretare e applicare tali regole (talora di fatto creandone di ulteriori), quali le pubbliche amministrazioni e il potere giudiziario. Vi sono poi gli organismi indipendenti che, in m…

ISTITUZIONI; regolazio; autorità indipendentiISTITUZIONIautorità indipendentiregolazioistituzioni regolazione potere politica istituzioni pubblica amministrazione autorità indipendenti
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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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Leach-Proof Sol–Gel Microcapsules as Curing Agents for One-Pot Thermosetting Resins

2013

The sol-gel microencapsulation of free-radical initiator benzoyl peroxide in sol-gel methyl-modified silica microcapsules of core/shell geometry allows curing of acrylate-based polyurethane and polyester resin formulations sprayed from a pressurized can without the need to compartmentalize reactants from the initiator to cross-link. These results open the route to widespread application of sol-gel microcapsules to efficiently cure polymer and composite mixtures that are widely used as functional coatings, molding compounds, adhesives, and sealants.

Polyester resinMaterials scienceGeneral Chemical EngineeringFunctional coatingThermosetting polymerBenzoyl peroxidechemistry.chemical_compoundPolymer chemistrySol-gelsmedicineEnvironmental ChemistryCuring agentsCuringSol-gel processMicroencapsulationCore/shellCuring (chemistry)PolyurethaneOne potchemistry.chemical_classificationAcrylateBenzoyl peroxideFree radical polymerizationProtective coatingsRenewable Energy Sustainability and the EnvironmentFree radical initiatorsGeneral ChemistryPolymerThermosetsMicrocapsuleschemistryChemical engineeringAdhesivemedicine.drugACS Sustainable Chemistry & Engineering
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Annelated pyrrolo-pyrimidines from amino-cyanopyrroles and BMMAs as leads for new DNA-interactive ring systems.

2005

The efficient one-pot synthesis of several new tricyclic systems of type 1 and 2, obtained from the reaction of substituted 2-amino-3-cyanopyrroles and 3-amino-4-cyanopyrroles with BMMAs, is reported. The duration and yields of the reaction strongly depend on the reactivity of the starting pyrrole and on the size of the ring to be formed. Mechanist features of the reaction were investigated and proposed by studying also the reactivity of a 3-aminopyrrole-2,4-dicyano substituted. The method reported represents the first example of the use of BMMA reagents in combination with pyrrole derivatives and allows an easy and versatile entry to a large number of hitherto unknown pyrrolo-pyrimidines f…

StereochemistryClinical BiochemistryPharmaceutical ScienceRing (chemistry)Annelated pyrrolo-pyrimidineBiochemistryChemical synthesisPyrrole derivativeschemistry.chemical_compoundBMMA reagentDrug DiscoveryReactivity (chemistry)PyrrolesMolecular BiologyPyrroleSpectrum AnalysisOrganic ChemistryDNAAmino-cyanopyrroleCombinatorial chemistryPyrimidineschemistryDNA-interactive polycycles.ReagentOne pot reactionMolecular MedicineDNABioorganicmedicinal chemistry
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