Search results for "eetterit"

showing 7 items of 7 documents

Deoxygenative Divergent Synthesis : En Route to Quinic Acid Chirons

2020

The installation of vicinal mesylate and silyl ether groups in a quinic acid derivative generates a system prone for stereoselective borane-catalyzed hydrosilylation through a siloxonium intermediate. The diversification of the reaction conditions allowed the construction of different defunctionalized fragments foreseen as useful synthetic fragments. The selectivity of the hydrosilylation was rationalized on the basis of deuteration experiments and computational studies. peerReviewed

Hydrosilylation010402 general chemistry01 natural sciencesBiochemistrySilyl etherchemistry.chemical_compoundredox reactionsPhysical and Theoretical Chemistryhapetus-pelkistysreaktioorgaaniset yhdisteeteetteritkemiallinen synteesi010405 organic chemistryreaction productsOrganic ChemistryhydrosilylationQuinic acidCombinatorial chemistry0104 chemical sciencesbond cleavageetherschemistryStereoselectivitySelectivityDivergent synthesisDerivative (chemistry)Vicinal
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Di- and Tetrairon(III) μ-Oxido Complexes of an N3S-Donor Ligand: Catalyst Precursors for Alkene Oxidations

2019

The new di- and tetranuclear Fe(III) μ-oxido complexes [Fe 4 (μ-O) 4 (PTEBIA) 4 ](CF 3 SO 3 ) 4 (CH 3 CN) 2 ] (1a), [Fe 2 (μ-O)Cl 2 (PTEBIA) 2 ](CF 3 SO 3 ) 2 (1b), and [Fe 2 (μ-O)(HCOO) 2 (PTEBIA) 2 ](ClO 4 ) 2 (MeOH) (2) were prepared from the sulfur-containing ligand (2-((2,4-dimethylphenyl)thio)-N,N-bis ((1-methyl-benzimidazol-2-yl)methyl)ethanamine (PTEBIA). The tetrairon complex 1a features four μ-oxido bridges, while in dinuclear 1b, the sulfur moiety of the ligand occupies one of the six coordination sites of each Fe(III) ion with a long Fe-S distance of 2.814(6) A. In 2, two Fe(III) centers are bridged by one oxido and two formate units, the latter likely formed by methanol oxidati…

MECHANISMFe-S interactionoxidation116 Chemical sciencesThio-rautaSULFURHomogeneous catalysis02 engineering and technology010402 general chemistry01 natural sciencesMedicinal chemistrythioetherCatalysislcsh:Chemistrychemistry.chemical_compoundThioetheriron-oxo complexAcetonitrileta116Fe-S interaction; homogeneous catalysis; iron-oxo complex; oxidation; thioetherOriginal Researchchemistry.chemical_classificationeetteritFUNCTIONAL-MODELCOORDINATIONPEROXIDEAlkeneLigandACTIVE-SITEhapettuminenGeneral Chemistrykompleksiyhdisteet021001 nanoscience & nanotechnology540COPPER-COMPLEXEShomogeneous catalysis0104 chemical sciencesChemistrychemistrylcsh:QD1-999katalyysiACIDOXO0210 nano-technologySelectivityNONHEME IRON CATALYSTSFrontiers in Chemistry
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Syntheses of Trifluoroethylated N-Heterocycles from Vinyl Azides and Togni’s Reagent Involving 1,n-Hydrogen-Atom Transfer Reactions

2020

2,2,2-Trifluoroethyl-substituted 3-oxazolines, 3-thiazolines, and 5,6-dihydro-2H-1,3-oxazines have been obtained by reacting substituted vinyl azides with a combination of Togni’s reagent and substoichiometric amounts of iron(II) chloride. The results of density functional theory calculations support the proposed mechanism involving 1,n-hydrogen-atom transfer reactions. peerReviewed

eetteritenergia010405 organic chemistryChemistryOrganic ChemistryreagentsHydrogen atom010402 general chemistry01 natural sciencesBiochemistryChloride0104 chemical sciencesetherssubstituentsReagentredox reactionsPolymer chemistryreagenssitmedicineDensity functional theoryPhysical and Theoretical Chemistryenergymedicine.drugOrganic Letters
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Chalcogen‐Bonding Interactions in Telluroether Heterocycles [Te(CH2)m]n (n=1-4; m=3-7)

2020

The Te…Te secondary bonding interactions (SBI) in solid heterocyclic telluroethers were explored by preparing and structurally characterizing a series of [Te(CH2)m]n (n = 1‐4; m = 3‐7) species. The SBIs in 1,7‐Te2(CH2)10, 1,8‐Te2(CH2)12, 1,5,9‐Te3(CH2)9, 1,8,15‐Te3(CH2)18, 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)28 led to the tubular packing of the molecules, as has been observed previously for related thio‐ and selenoether rings. The nature of the intermolecular interactions was explored by solid‐state PBE0‐D3/pob‐TZVP calculations involving periodic boundary conditions. The packing of molecules in 1,7,13,19‐Te4(CH2)20, 1,8,15,22‐Te4(CH2)24, and 1,9,17,25‐Te4(CH2)…

eetteritheterocyclesnoncovalent interactionskemialliset sidoksettelluuritelluriumdensity functional calculationssolid-state structurestiheysfunktionaaliteoriaorganometalliyhdisteet
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Ion pair recognition by ditopic crown ether based bis-urea and uranyl salophen receptors

2016

ionition pair bindingcrown ethersuranyl salophensureatitraussupramolecular chemistryditopic receptorsionisidosanion bindinguranyylisalofeenitkemialliset sidoksetkruunueetteritsupramolekyylikemia¹H NMR titrationsNMR-spektroskopiaorgaaniset yhdisteetröntgenkristallografiaX-ray crystallography
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Selective Synthesis of Z -Silyl Enol Ethers via Ni-Catalyzed Remote Functionalization of Ketones

2021

Journal of the American Chemical Society : JACS 143(22), 8375-8380 (2021). doi:10.1021/jacs.1c01797

ketonesSilylationDimerketonit010402 general chemistry01 natural sciencesBiochemistrytransition metalsCatalysisCatalysischemistry.chemical_compoundkatalyytitColloid and Surface ChemistryPolymer chemistryhydrocarbonsoligomerseetteritkemiallinen synteesiOlefin fiberGeneral ChemistrySilyl enol ether540Enolhiilivedyt3. Good health0104 chemical sciencesoligomeerietherschemistryChain walkingddc:540nikkeliSelectivityJournal of the American Chemical Society
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Tiokruunueetterien metallikompleksit

2012

Tämä LuK-tutkielma käsittelee tiokruunueetterien metallikomplekseja. Tarkemman tarkastelun kohteeksi on valittu pelkkiä rikkidonoreita sisältävien tiokruunueettereiden hopea-, kulta-, kupari-, palladium- ja platinakompleksit, jotka ovat lisäksi homoleptisiä eli eivät sisällä tiokruunueetterien lisäksi muita ligandeja. Tutkielmassa on keskitetty lähinnä kompleksien rakenteisiin ja koordinaatiokemiaan.

tiokruunueetteritrikkidonoritmetallikompleksit
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