Search results for "arrangement."

showing 10 items of 343 documents

Luogo di sosta al Largo delle Grotte

2020

Testo di presentazione e progetto architettonico realizzato nell’ambito di una ricerca interdipartimentale sul centro storico di Caltabellotta. L’intervento riguarda la sistemazione di un’area scenografica della città in cui i temi della natura e dell’archeologia vengono interpretati e restituiti da una soluzione architettonica.

Settore ICAR/14 - Composizione Architettonica E UrbanaPresentation text and architectural project carried out as part of an interdepartmental research on the historic center of Caltabellotta. The intervention concerns the arrangement of a scenic area of the city where the themes of nature and archeology are interpreted and returned by an architectural solution.
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Il Seminario greco-albanese di Palermo e la memoria documentaria delle comunità arbëreshe. Inventario

2021

Il contributo, nel presentare l'inventario dell'archivio storico del Seminario greco-albanese di Palermo (secc. XVIII-XX), illustra le vicende documentarie delle comunità arbëreshe di Sicilia. The contribution, in presenting the inventory of the historical archive of the Greek-Albanian Seminary of Palermo (XVIII-XX centuries), illustrates the documentary events of the Arbëreshe communities of Sicily.

Settore M-STO/08 - Archivistica Bibliografia E Biblioteconomiaarchivi storicihistorical archiverearrangementitalo-Albanesi: minoranzeArchiveriordinamentoItalian-Albanians: minoritieArchivi
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Some remarks on the extinction time for the mean curvature flow

2005

We write some consideratons on the extinction time for the mean curvature flow

Settore MAT/05 - Analisi MatematicaMean curvature flowrearrangementextinction time
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Computing the Arrangement of Circles on a Sphere, with Applications in Structural Biology

2009

International audience; Balls and spheres are the simplest modeling primitives after affine ones, which accounts for their ubiquitousness in Computer Science and Applied Mathematics. Amongst the many applications, we may cite their prevalence when it comes to modeling our ambient 3D space, or to handle molecular shapes using Van der Waals models. If most of the applications developed so far are based upon simple geometric tests between balls, in particular the intersection test, a number of applications would obviously benefit from finer pieces of information. Consider a sphere $S_0$ and a list of circles on it, each such circle stemming from the intersection between $S_0$ and another spher…

Single passSpheresControl and Optimization0102 computer and information sciences[INFO.INFO-CG]Computer Science [cs]/Computational Geometry [cs.CG]01 natural sciencesArrangement of circlesDockingmolecular surfacesCombinatorics03 medical and health sciencesVan der Waals modelsConformational ensembles030304 developmental biologyMathematics0303 health sciencesOptimization algorithmData structureComputer Science ApplicationsAlgebraComputational Mathematics[INFO.INFO-CG] Computer Science [cs]/Computational Geometry [cs.CG]Computational Theory and MathematicsStructural biology010201 computation theory & mathematicsBall (bearing)[ INFO.INFO-CG ] Computer Science [cs]/Computational Geometry [cs.CG]SPHERESGeometry and TopologyAffine transformationflexible docking
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A Theoretical Study of the Favorskii Rearrangement. Calculation of Gas-Phase Reaction Paths and Solvation Effects on the Molecular Mechanism for the …

1997

The molecular mechanism of the α-chlorocyclobutanone transposition to yield cyclopropanecarboxylic acid, as a model of the Favorskii rearrangement, has been theoretically characterized in vacuo by means of ab initio molecular orbital procedures at the Hartree−Fock (HF) level of theory with the 6-31G* and 6-31+G* basis sets. The electron correlation has been estimated at the MP2/6-31G* level and calculations based on density functional theory, BLYP/6-31G*. The solvent effects are included at HF/6-31G* level by means of a polarizable continuum model. The questions related to the two accepted molecular mechanisms, the semibenzilic acid and the cyclopropanone transpositions, as well as the comp…

SolvationAb initioThermodynamicsGeneral ChemistryFavorskii rearrangementBiochemistryPolarizable continuum modelCatalysischemistry.chemical_compoundColloid and Surface ChemistrychemistryComputational chemistryCyclopropanoneMolecular orbitalDensity functional theorySolvent effectsJournal of the American Chemical Society
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ChemInform Abstract: Photochemical Functionalization of Allyl Benzoates by C-H Insertion.

2013

The photoreactivity of allyl benzoates, containing an electron-rich double bond, has been explored by irradiation at 305 nm in different solvents. Solvent addition products arising from an insertion of the alpha H–C bonds of THF, dioxane, and i-PrOH to the allylic double bond was realized. The observed reactivity depended on reaction conditions and substitution pattern of the substrate. A DFT study on this unusual reaction was performed allowing the formulation of two mechanistic pathways.

SolventReaction conditionschemistry.chemical_classificationAllylic rearrangementDouble bondchemistrySubstrate (chemistry)Surface modificationReactivity (chemistry)General MedicinePhotochemistryBenzoatesChemInform
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Untersuchungen zurFriesschen Verschiebung von Estern derortho- undpara-Methoxybenzoes�ure

1979

TheFries rearrangement of different methoxy benzoates has been investigated. Frompara-methoxy benzoates the corresponding hydroxy-4′-methoxy benzophenones could be obtained in good yields by treatment withLewis acids (especially TiCl4) in nitromethane at 20°C (4-hydroxy derivatives) or without solvent at 120°C (2-hydroxy derivatives). Under the same conditions only demethylation occurs withortho-methoxy benzoates leading to the corresponding salicylates. Small amounts of hydroxy-2′-methoxy benzophenones were obtained by treatment with polyphosphoric acid.

Solventchemistry.chemical_compoundNitromethaneFries rearrangementChemistryOrganic chemistryGeneral ChemistryBenzoatesDemethylationMonatshefte f�r Chemie
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A new palladium(II)-catalyzed [3,3] aza-Claisen rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles

2011

Abstract A new efficient palladium(II)-catalyzed [3,3] aza-Claisen, formal sigmatropic rearrangement of 3-allyloxy-5-aryl-1,2,4-oxadiazoles was developed. The mechanism was studied by analyzing the regiochemical and stereochemical course of the reaction. The results obtained indicated the intervention of a cationic pallada-cycle similar to the one postulated for the Cope rearrangement of 1,5-dienes.

StereochemistryArylOrganic ChemistryCationic polymerizationchemistry.chemical_elementSettore CHIM/06 - Chimica OrganicaSigmatropic reactionBiochemistryCarroll rearrangementAza-Claisen 124-Oxadiazoles 124-Oxadiazolones PalladiumCatalysisClaisen rearrangementchemistry.chemical_compoundchemistryDrug DiscoveryPalladiumCope rearrangement
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A deep insight into the mechanism of the acid-catalyzed rearrangement of the Z-phenylhydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole in a non-polar s…

2010

The conversion of the Z-phenylhydrazone of 5-amino-3-benzoyl-1,2,4-oxadiazole (1a) into the relevant 1,2,3-triazole (2a) has been quantitatively studied in toluene in the presence of several halogenoacetic acids (HAAs, 3a–h). Again, the occurrence of two reaction pathways has been pointed out: they require one or two moles of acid, respectively, thus repeating the situation previously observed in the presence of trichloroacetic acid. The observed rate constant ratios (kIII/kII) are only slightly affected by the nature of the acid used. To gain a deeper insight into the action of the acids used we have measured the association constants of the HAAs (3a–h) with 4-nitroaniline (4) in toluene. …

StereochemistryOrganic ChemistryOxadiazoleSettore CHIM/06 - Chimica OrganicaTolueneMedicinal chemistrySolventchemistry.chemical_compoundAcid catalysisReaction rate constantchemistryAcid catalyzedMoleAcid catalysis azoles mononuclear rearrangement of heterocycles ring to ring interconversionPhysical and Theoretical ChemistryTrichloroacetic acidJournal of Physical Organic Chemistry
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Allylpalladium( II ) Complexes with Aminophosphane Ligands: Solution Behaviour and X‐ray Structure of cis ‐[Pd(η 3 ‐CH 2 CHCHPh){Ph 2 PCH 2 CHPhNH(2,…

2004

A new β-aminophosphane L2 [Ph2PCH2CH(Ph)NH(2,6-C6H3iPr2)], bearing an asymmetric carbon atom and a vicinal prochiral nitrogen centre and (η3-allyl)palladium complexes of general formula [Pd(η3-C3H4R){η2-Ph2PCH2CH(Ph)NHAr}][PF6] (1−6) (R = H, Me or Ph and Ar = Ph or 2,6-C6H3iPr2) have been synthesised. NMR spectroscopic studies and a crystal structure analysis of complex 6 (R = Ph, Ar = 2,6-C6H3iPr2) confirmed the highly diastereoselective coordination of the nitrogen atom. Because of the allyl fluxionality and the presence of asymmetric centres, all the complexes exist in solution as mixtures of up to four diastereomers. For the monosubstituted allyl complexes [Pd(η3-C3H4R){Ph2PCH2CH(Ph)NHA…

Steric effectsAllylic rearrangement010405 organic chemistryChemistryStereochemistryDiastereomerRegioselectivityCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryAsymmetric carbonMoietyIsomerizationEuropean Journal of Inorganic Chemistry
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