Search results for "cycles"

showing 10 items of 306 documents

Switchable Access to Different Spirocyclopentane Oxindoles by N-Heterocyclic Carbene Catalyzed Reactions of Isatin-Derived Enals and N-Sulfonyl Ketim…

2017

A novel NHC-catalyzed annulation protocol for the asymmetric synthesis of biologically important β-lactam fused spirocyclopentane oxindoles with four contiguous stereocenters, including two quaternary carbon centers, was developed. Alternatively, spirocyclopentane oxindoles containing an enaminone moiety can be achieved using the same starting materials, isatin-derived enals, and N-sulfonyl ketimines, in the presence of a slightly different NHC catalytic system. This switchable annulation strategy enables the selective assembly of both heterocyclic scaffolds with good yields and excellent enantioselectivities for a broad range of substrates.

Annulationasymmetric synthesis010402 general chemistry01 natural sciencesCatalysisStereocenterchemistry.chemical_compoundkatalyytitMoietyOrganic chemistryorganocatalysisN-heterocyclic carbenesheterosykliset yhdisteetspiro-compoundsta116Sulfonylchemistry.chemical_classificationkemiallinen synteesiheterocycles010405 organic chemistryIsatinEnantioselective synthesisGeneral ChemistryGeneral Medicine0104 chemical scienceschemistryOrganocatalysisCarbeneAngewandte Chemie
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Efficient two-step synthesis of face-to-face meso-substituted bis(corrole) dyads

2008

The synthesis of face-to-face meso-substituted bis(corrole) systems was revisited. By using a new synthetic pathway, the reaction was generalized to any type of linker and the yield was considerably increased. The dyads were obtained in yields up to 20 % from a dialdehyde linker and dipyrromethane in a one-step reaction. The best reaction conditions required a decreased amount of TFA catalyst (1.4 equiv.) and a large excess of dipyrromethane (up to 8 equiv). Under these conditions, four bis(corrole)s linked by 2,2′-diphenyl ether, 9,9-dimethylxanthene, anthracene, and dibenzofuran spacers were synthesized.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

Anthracene010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic ChemistryTwo stepEther010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisDibenzofuranchemistry.chemical_compoundmacrocycleschemistry[ CHIM.ORGA ] Chemical Sciences/Organic chemistryYield (chemistry)Polymer chemistrysynthetic methodsPhysical and Theoretical ChemistryCorrolecorrolesLinkerComputingMilieux_MISCELLANEOUS
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Marine Pyrrole Alkaloids

2021

Nitrogen heterocycles are essential parts of the chemical machinery of life and often reveal intriguing structures. They are not only widespread in terrestrial habitats but can also frequently be found as natural products in the marine environment. This review highlights the important class of marine pyrrole alkaloids, well-known for their diverse biological activities. A broad overview of the marine pyrrole alkaloids with a focus on their isolation, biological activities, chemical synthesis, and derivatization covering the decade from 2010 to 2020 is provided. With relevant structural subclasses categorized, this review shall provide a clear and timely synopsis of this area.

Aquatic OrganismsQH301-705.5Ecologymarine natural productsPharmaceutical Sciencepyrrole-aminoimidazole alkaloidsReviewBiologyalkaloidsStructure-Activity Relationshipchemistry.chemical_compoundchemistrypyrrolesDrug DiscoveryAnimalspyrrole-imidazole alkaloidsnitrogen heterocyclesbromopyrrolesBiology (General)Pharmacology Toxicology and Pharmaceutics (miscellaneous)PyrroleMarine Drugs
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Partitioning of macrocyclic compounds in a cationic and an anionic micellar solution: a small-angle neutron scattering study.

2004

Following a previous investigation on partitioning of some macrocycle compounds in sodium dodecyl sulfate (SDS) and dodecyltrimethylammonium bromide (DTAB) aqueous solutions and their effect on the micellar structure, a small-angle neutron scattering (SANS) study has been performed at fixed surfactant content (0.20 mol/L) and varying macrocycle concentrations from 0.20 up to 1.0 mol/L. Conductivity measurements have been also performed in order to evaluate the effect of the presence of macrocycles on the critical micellar concentration (cmc) of the two surfactants. SANS experimental data were fitted successfully by means of a core-plus-shell monodisperse prolate ellipsoid model. It has been…

Aqueous solutionChemistryCationic polymerizationSurfactants Macrocycles SANSSurfaces and InterfacesNeutron scatteringCondensed Matter PhysicsMicelleSmall-angle neutron scatteringCrystallographychemistry.chemical_compoundPulmonary surfactantCritical micelle concentrationElectrochemistryPhysical chemistryGeneral Materials ScienceSodium dodecyl sulfateSpectroscopyLangmuir : the ACS journal of surfaces and colloids
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[2]Catenanes and inclusion complexes derived from self-assembled rectangular PdII and PtII metallocycles

2012

New inclusion complexes and [2]catenanes were self-assembled from a fluorescent diazapyrenium based ligand, a PdII or PtII complex, and cyclic or acyclic electron rich aromatic guests in aqueous and organic media. The molecular rectangles display a π-deficient cavity suitable to incorporate π-donor aromatic systems. The inclusion complexes between the metallocycles and phenylenic (2a,b) and naphthalenic (3a,b–5a,b) derivatives were studied by NMR, UV-vis and fluorescence spectroscopy. The crystal structure of (3b) ⊂ 1a·6PF(6) confirmed the insertion of the guest into the cavity of the metallocycle. Following the same self-assembly strategy, the use of polyethers 6,7 as π-donors resulted in …

Aqueous solutionLigandChemistryStereochemistryCatenaneCrystal structureSettore CHIM/06 - Chimica OrganicaMetallacycleFluorescenceFluorescence spectroscopySelf assembledCatenanes inclusion complexes PdII PtII metallocyclesInorganic ChemistryCrystallographySettore CHIM/03 - Chimica Generale E Inorganica
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Complexation and Extraction of PAHs to the Aqueous Phase with a Dinuclear Pt II Diazapyrenium‐Based Metallacycle

2010

New palladium and platinum metallacycles have been synthesized by reaction between a 2,7-diazapyrenium-based ligand and Pd(II) and Pt(II) complexes. The inclusion complexes between the metallacycles and polycyclic aromatic hydrocarbons (PAHs) in CD(3)NO(2) and D(2)O were studied by NMR spectroscopy. The structures of the inclusion complexes of the Pt metallacycle as host with pyrene, phenanthrene, and triphenylene were confirmed by single crystal X-ray crystallography. The association constants between the Pt metallacycle and the selected PAHs were determined in CH(3)CN following the characteristic charge-transfer band displayed in their UV/Vis absorption spectrum. Although in aqueous solut…

Aqueous solutionLigandOrganic Chemistrychemistry.chemical_elementTriphenyleneGeneral ChemistryNuclear magnetic resonance spectroscopyMetallacyclePhotochemistryMedicinal chemistryCatalysisJob plotchemistry.chemical_compoundchemistryPyreneinclusion compounds metallacycles polycyclic aromatic hydrocarbons self-assembly supramolecular chemistryPalladiumChemistry – A European Journal
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Polyfunctional Tetraaza-Macrocyclic Ligands: Zn(II), Cu(II) Binding and Formation of Hybrid Materials with Multiwalled Carbon Nanotubes

2017

The binding properties of HL1, HL2, and HL3 ligands toward Cu(II) and Zn(II) ions, constituted by tetraaza-macrocyclic rings decorated with pyrimidine pendants, were investigated by means of potentiometric and UV spectrophotometric measurements in aqueous solution, with the objective of using the related HL-M(II) (HL = HL1–HL3; M = Cu, Zn) complexes for the preparation of hybrid MWCNT-HL-M(II) materials based on multiwalled carbon nanotubes (MWCNTs), through an environmentally friendly noncovalent procedure. As shown by the crystal structure of [Cu(HL1)](ClO4)2, metal coordination takes place in the macrocyclic ring, whereas the pyrimidine residue remains available for attachment onto the s…

Aqueous solutionMaterials sciencePyrimidine010405 organic chemistryGeneral Chemical EngineeringInorganic chemistryPotentiometric titrationStackingGeneral ChemistryCrystal structure010402 general chemistryRing (chemistry)01 natural sciencesArticle0104 chemical sciencesMetallcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999visual_artPolymer chemistryvisual_art.visual_art_mediumHybrid materialcarbon nanotubes copper zinc macrocycles hybrid materials functionalized carbon nanotubesACS Omega
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Milankovitch forcing of Early Jurassic wildfires

2019

The Early Jurassic was characterized by major climatic and environmental perturbations which can be seen preserved at high resolution on orbital timescales. The Early Jurassic is a period of overall global warmth, and therefore serves as a suitable modern-day analogue to understand changes in the Earth System. Presently, Earth’s climate is warming and the frequency of large wildfires appears to be increasing. Recent research has indicated that Quaternary deposits reveal that wildfires respond to orbital forcings; however, to date no study has been able to test whether wildfire activity corresponds to changes over Milankovitch timescales in the deep past. A high-resolution astrochronology ex…

AstrochronologyMilankovitch cyclesOrbital forcingSedimentary rockPhysical geographyVegetationForcing (mathematics)QuaternaryMonsoonGeology
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Preparation and Characterization of P2 BCh Ring Systems (Ch=S, Se) and Their Reactivity with N-Heterocyclic Carbenes

2018

Four-membered rings with a P2BCh core (Ch = S, Se) have been synthesized via reaction of phosphinidene chalcogenide (Ar*P=Ch) and phosphaborene (Mes*P=BNR2). The mechanistic pathways towards these rings are explained by detailed computational work that confirmed the preference for the formation of P–P, not P–B, bonded systems, which seems counterintuitive given that both phosphorus atoms contain bulky ligands. The reactivity of the newly synthesized heterocycles, as well as that of the known (RPCh)n rings (n = 2, 3), was probed by the addition of Nheterocyclic carbenes, which revealed that all investigated compounds can act as sources of low-coordinate phosphorus species. peerReviewed

BOND COVALENT RADIIChalcogenidePHOSPHINIDENE ADDUCTSSULFURchemistry.chemical_element010402 general chemistryRing (chemistry)ION ABSTRACTION01 natural sciencesMedicinal chemistryCatalysischemistry.chemical_compoundELEMENTSmain-group heterocyclesReactivity (chemistry)N-heterocyclic carbenesMETHYLENEPHOSPHINEta116epäorgaaniset yhdisteetphosphinidene chalcogenidesheterocycleskemiallinen synteesiphosphaborenes010405 organic chemistryPhosphorusOrganic ChemistryGeneral ChemistryREAGENT0104 chemical sciencesCharacterization (materials science)PHOSPHORUSchemistryPhosphinideneinorganic compoundsSULFURIZATIONchemical synthesisX-RAY-STRUCTUREChemistry - A European Journal
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Wesley Mitchell, Arthur Burns and Trygve Haavelmo on business cycles The two Encyclopaedia of the social sciences (1930–1935 and 1968)

2012

The paper presents a brief reconstruction of the history of the Encyclopaedia of the Social Sciences (1930-1935 and 1968) a 15 volume major editorial enterprise that was accomplished under the direction of Columbia economist E.R.A. Seligman. It then provides an analysis of the main entries that were devoted to business cycle theory, namely those by Wesley C. Mitchell, Arthur Burns and Trygve Haavelmo.

BUSINESS CYCLESSettore SECS-P/04 - Storia Del Pensiero Economico
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