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showing 10 items of 25093 documents

Gold-Catalyzed Povarov-Type Reaction of Fluorinated Imino Esters and Furans

2016

A gold-catalyzed Povarov-type reaction of fluorinated imino esters and furans is described. The process, which takes place in dichoromethane at room temperature, gives rise to novel fluorinated tetrahydrofuran-fused tetrahydroquinolines in good yields and moderate levels of diastereo-selectivity in a very simple manner. The reported examples expand the versatility of the Povarov reaction to unprecedented fluorinated substrates, generating scaffolds that contain quaternary alpha-amino acid units.

010405 organic chemistryChemistryOrganic ChemistryOrganic chemistryPovarov reaction010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisThe Journal of Organic Chemistry
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Mononuclear Rearrangement of the Z-Phenylhydrazones of Some 3-Acyl-1,2,4-oxadiazoles: Effect of Substituents on the Nucleophilic Character of the &gt…

2019

The reaction rates for the mononuclear rearrangement of the Z-phenylhydrazones of 3-acyl-1,2,4-oxadiazoles 3a-c into the relevant 2-phenyl-2 H-1,2,3-triazoles (4a-c) have been measured in dioxane/water at different temperatures in a large range of proton concentrations. The occurrence of two different reaction pathways (one uncatalyzed, water assisted, and the other general base catalyzed) has- been observed. The obtained results have been able to furnish information about the effects of the nature of the 3-acyl structure and of the 5-substituents in the 1,2,4-oxadiazole ring on the reactivity of the examined rearrangements: they are well in line with the previsions carried out considering …

010405 organic chemistryChemistryOrganic ChemistryOxadiazoleCharge density010402 general chemistryRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisReaction ratechemistry.chemical_compoundNucleophileElectrophileReactivity (chemistry)The Journal of Organic Chemistry
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Interactions of a Diplumbyne with Dinuclear Transition Metal Carbonyls to Afford Metalloplumbylenes

2020

The metathesis reactions of the diplumbyne AriPr6PbPbAriPr6 (AriPr6 = −C6H3–2,6-(C6H2–2,4,6-iPr3)2) with the dinuclear metal carbonyls Mn2(CO)10, Fe2(CO)9, and Co2(CO)8 under mild conditions afforded the complexes Mn(CO)5(PbAriPr6) (1), Fe(CO)4(PbAriPr6)2 (2), and Co4(CO)9(PbAriPr6)2 (3), respectively. Complexes 1–3 were structurally characterized by single-crystal X-ray diffraction and spectroscopically characterized by 1H, 13C{1H}, 59Co{1H}, and 207Pb{1H} NMR; UV–vis; and IR methods. They are rare examples of species formed by the direct reaction of a group 14 dimetallyne with transition metal carbonyls. Complexes 1 and 2 feature Mn–Pb or Fe–Pb single bonds, whereas in 3 a Co–Pb cluster i…

010405 organic chemistryChemistryOrganic ChemistrycarbonylsmetalsMetal carbonylkompleksiyhdisteetorganometalliyhdisteet010402 general chemistry01 natural sciencescobalttransition metals0104 chemical sciencesInorganic ChemistryTransition metalPolymer chemistrySalt metathesis reactionPhysical and Theoretical Chemistrykarbonyylitnuclear magnetic resonance spectroscopy
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Organocatalytic enantioselective Strecker reaction with seven-membered cyclic imines

2018

[EN] A highly enantioselective Strecker reaction with dibenzo[b,f][1,4]oxazepines has been described using a dihydroquinine-derived thiourea as organocatalyst. The reaction affords chiral 10,11-dihydrodibenzo[b,f][1,4] oxazepine 11-carbonitrile derivatives in excellent yields (up to 99%) and excellent enantioselectivities (up to 98%) under mild reaction conditions.

010405 organic chemistryChemistryOrganocatalysisDibenzo[bf][14]oxazepinesStrecker amino acid synthesisEnantioselective synthesisGeneral Chemistry010402 general chemistry01 natural sciences0104 chemical sciencesReaccions químiquesAlpha-amino nitrilesCatàlisiStrecker reactionOrganocatalysisFISICA APLICADAAsymmetric catalysisEconomic historymedia_common.cataloged_instanceEuropean unionmedia_common
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Vinyl Fluorides: Competent Olefinic Counterparts in the Intramolecular Pauson–Khand Reaction

2019

Despite the great advances achieved in the Pauson-Khand reaction and the ever-increasing demand for fluorinated compounds, the use of vinyl fluorides as olefinic counterparts in the above-mentioned transformation had been completely overlooked. Herein, we describe, for the first time, the intramolecular Pauson-Khand reaction of enynes containing a vinyl fluoride moiety.

010405 organic chemistryChemistryPauson–Khand reactionOrganic Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical scienceschemistry.chemical_compoundIntramolecular forcePolymer chemistryMoietyPhysical and Theoretical ChemistryVinyl fluorideOrganic Letters
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Theoretical Investigation of the Low-Energy States of CpMoCl(PMe 3 ) 2 and Their Role in the Spin-Forbidden Addition of N 2 and CO

2003

International audience; A recent computational investigation of Jahn−Teller effects in unsaturated 16-electron d4d6 [CpMLn] complexes (Abu-Hasanayn, F.; Cheong, P.; Oliff, M. Angew. Chem.2002, 41, 2120) highlighted the typical presence of two spin-triplet and two singlet states of competing stability in these complexes and pointed out the necessity to account for more than one electronic state in studies thereof. Consequently, we have reinvestigated the addition of N2 to all the four low-energy states of CpMoCl(PH3)2, a reaction for which previously only one singlet and one triplet state have been considered (Keogh, D. W.; Poli, R. J. Am. Chem. Soc.1997, 119, 2516). The present study was pe…

010405 organic chemistryChemistryState (functional analysis)010402 general chemistry01 natural sciencesQuantum mechanics0104 chemical sciencesElectronic statesAddition reactionsChemical calculations[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryLow energyChemical structureMathematical methodsDensity functional theory[CHIM.COOR]Chemical Sciences/Coordination chemistrySinglet statePhysical and Theoretical ChemistryAtomic physicsTriplet statePhysics::Chemical PhysicsSpin (physics)Ground state
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Half-sandwich complexes of molybdenum-(III), -(IV) and -(V) with P–O and P–N bifunctional ligands Ph2PCH2X (X = 2-oxazolinyl, or C(O)NPh2)

2000

International audience; The reaction of the ligands Ph2PCH2X (X = 2-oxazolinyl, I; or C(O)NPh2, II) with the half-sandwich molybdenum(III) precursors [Mo(η-C5R5)(μ-Cl)2]2 (R = H or Me) has been investigated. Ligand I reacts with both complexes to form the corresponding adducts [Mo(η-C5R5)Cl2(Ph2PCH2C3H4NO)] (R = H, 1; or Me, 2). The reaction between I and [MoCp*Cl4] (Cp* = η-C5Me5) affords [MoCp*Cl4(Ph2PCH2C3H4NO-κ1P)] as a kinetic isomer, which then transforms quantitatively to [MoCp*Cl3(Ph2PCH2C3H4NO-κ2P,N)]+Cl−, 3. Ligand II reacts with [MoCp(μ-Cl)2]2 (Cp = η-C5H5) to afford the adduct [CpMoCl2{Ph2PCH2C(O)NPh2-κ2P,O}], 4, as an equilibrium mixture of two isomers. Longer reaction times in…

010405 organic chemistryChemistryStereochemistryLigandIonic bondingchemistry.chemical_elementGeneral Chemistry010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesAdductchemistry.chemical_compoundMolybdenum[CHIM.COOR]Chemical Sciences/Coordination chemistryDirect reactionBifunctionalSingle crystal
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The Fluoro-Pauson-Khand Reaction in the Synthesis of Enantioenriched Nitrogenated Bicycles Bearing a Quaternary C-F Stereogenic Center

2019

The authors are grateful to the Spanish MICINN and the AEI (CTQ2017-84249-P) for financial support, the SCSIE (Universitat de Valencia) for access to instrumental facilities, and M. ̀ R. Pedrosa (Universidad de Burgos) for providing us with MoO2Cl2. The technical and human support provided by SGIker (UPV/EHU, MINECO, GV/DJ, ERDF, and ESF) is also gratefully acknowledged. P.B. thanks the Spanish Ministry of Economy for a Ramon y Cajal contract (RyC-2016-20951). ́ The authors are also grateful to Jose Cabeza for assistance in the synthesis of certain starting materials.

010405 organic chemistryChemistryStereochemistryPauson–Khand reactionOrganic ChemistryPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesStereocenter
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From self-inclusion and host-guest complexes to channel structures

2012

Various supramolecular interactions are applied as driving forces in self-assembly and molecular recognition processes. Single crystal X-ray diffraction method is especially important for solid-state studies of non-covalent interactions as it reveals their influence on the molecular and supramolecular structures. This paper discusses structures of two completely different types of compounds in which a variety of intermolecular interactions are involved. It will be shown that strong and weak intermolecular hydrogen bonds in N-alkylammonium resorcinarene salts, depending on the type of anion, inclusion of resorcinarene upper rim pendant group or solvent molecules into the cavity, strongly aff…

010405 organic chemistryChemistryStereochemistryX-ray structure; supramolecular chemistry; hydrogen bonding; hydrophobic interaction; resorcinarene; palladium complexSupramolecular chemistryGeneral ChemistryInclusion (mineral)010402 general chemistryta11601 natural sciencesHost (network)0104 chemical sciencesCommunication channel
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Towards the synthesis of substituted porphyrins by a pyridyl group bearing a reactive functionality

2010

Pyridyl-substituted porphyrins bearing a reactive functionality were prepared via Suzuki cross-coupling reactions and resulted in very good yields. These compounds are precursors of new porphyrin architectures able to coordinate two metals: one in the porphyrin core and the second around the pyridyl moiety. During the coupling reactions, a higher reactivity of a chloro picolyl group was evidenced compared to a bromo function on the same reacting molecule.

010405 organic chemistryChemistryStereochemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryGeneral Chemistry010402 general chemistry01 natural sciencesPorphyrinCoupling reaction0104 chemical sciencesA3B-porphyrinschemistry.chemical_compoundSuzuki reactionGroup (periodic table)[ CHIM.ORGA ] Chemical Sciences/Organic chemistryPolymer chemistrypolycyclic compoundsMoietyMoleculeheterocyclic compoundsReactivity (chemistry)meso-functionalizationSuzuki couplingpyridyl substituted porphyrinsComputingMilieux_MISCELLANEOUS
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