Search results for "Fig"

showing 10 items of 1359 documents

Crateri-cinerari figurati in Sicilia:immagini, rito e credenze religiose

2007

La dialettica tra sfera del vino e sfera della morte caratterizza le culture occidentali, greche, anelleniche e grecizzate, e si configura quasi come elemento identificativo di alcuni contesti socio-culturali di frontiera. La netta opposizione tra simposio e ambito funerario, che distingue l’ambiente greco, si trasforma nelle comunità etrusche, italiche e coloniali dinamica associazione ricca di sottesi valori simbolici ed escatologici. La tematica, pur essendo già esplorata, viene ripresa in tale contributo, nel quale si suggeriscono nuovi accorpamenti e letture combinate di documenti, che nel loro insieme, seppure disomogeneo, possono contribuire a spiegare fenomeni di devianze all’intern…

ceramica figurata necropoli siceliote DionisoSettore L-ANT/07 - Archeologia Classica
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Something Borrowed : Interfigural Characterisation in Anglo-American Fantasy Comics

2016

It is no secret that comics’ formal structure resembles a pastiche: images, words and gaps of different styles and abstraction levels mix to tell a story that is more than their sum. Is it any wonder, then, that modern, myth-driven graphic novels tend to borrow their content elements – such as characters – from several heterogeneous sources as well? Wolfgang G. Müller's little-known but widely applicable theory of interfigurality (1991) shows how literary characters gain depth and resonance by sharing elements with characters in other works. The chapter revises his theory and shows how it could also be used in the analysis of comic book characters. Fantasy comics from Vertigo series like Fa…

character theoryVertigo comicssarjakuvahahmotinterfiguralityintertekstuaalisuusfiktiiviset hahmotcognitive theoryfantasia (tyylit)transmedialitysarjakuvat
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Synthesis of l -[4-11 C]Asparagine by Ring-Opening Nucleophilic 11 C-Cyanation Reaction of a Chiral Cyclic Sulfamidate Precursor

2018

The development of a convenient and rapid method to synthesize radiolabeled, enantiomerically pure amino acids (AAs) as potential positron emission tomography (PET) imaging agents for mapping various biochemical transformations in living organisms remains a challenge. This is especially true for the synthesis of carbon-11-labeled AAs given the short half-life of carbon-11 (11 C, t1/2 =20.4 min). A facile synthetic pathway to prepare enantiomerically pure 11 C-labeled l-asparagine was developed using a partially protected serine as a starting material with a four-step transformation providing a chiral five-membered cyclic sulfamidate as the radiolabeling precursor. Its structure and absolute…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryAbsolute configurationStereoisomerismGeneral ChemistryCyanation010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesAmino acidHydrolysisNucleophilechemistryYield (chemistry)AsparagineChemistry - A European Journal
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Acetogenins from Annonaceae

1997

In 1982, Jolad et al. isolated uvaricin, a new antitumor agent, from the roots of Uvaria acuminata (Annonaceae), a bis-tetrahydrofuranoid fatty acid lactone (1) related to polyketides or acetogenins. However, it contained a number of original structural characteristics, particularly a linear acetogenin, a bis-tetrahydrofuran pattern flanked by hydroxyls and a terminal unsaturated lactone. Two years later, Dabrah and Sneden (2, 3 and Cortes et al. (4) described four new products presenting the same structural characteristics. Because these products formed a new class of natural compounds, and are only found in species belonging to the family of Annonaceae, they are commonly called acetogenin…

chemistry.chemical_classificationAntitumor activitybiologyStereochemistryAbsolute configurationFatty acidbiology.organism_classificationUvaria acuminataUvaricinchemistry.chemical_compoundchemistryAnnonaceaeAcetogeninLactone
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Stereochemistry of terpene derivatives. Part 4:☆ Fragrant terpenoid derivatives with an unsaturated gem-dimethylbicyclo[3.1.0]hexane system

2005

Abstract Starting from (+)-3-carene 1 several chiral fragrant compounds with the bicyclo[3.1.0]hexane system 4–6 and 10–20 were synthesized. These compounds are structural analogues of naturally occurring fragrant compounds, such as ionones and damascones, and possess either an endo- or an exo-cyclic double bond in the bicyclo[3.1.0]hexane moiety. The absolute configuration of selected products was confirmed by X-ray crystallography and circular dichroism analysis.

chemistry.chemical_classificationCircular dichroismBicyclic moleculeDouble bondChemistryStereochemistryOrganic ChemistryAbsolute configurationCatalysisTerpenoidInorganic ChemistryTerpeneHexanechemistry.chemical_compoundMoietyOrganic chemistryPhysical and Theoretical ChemistryTetrahedron-Asymmetry
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Homochiral self-assembly of biocoordination polymers: anion-triggered helicity and absolute configuration inversion

2015

The different natures of the weakly coordinating anions – triflate or perchlorate – in the Cu2+-mediated self-assembly of cytidine monophosphate nucleotide play a fundamental role in the homochiral resolution process, yielding one-dimensional copper(II) coordination polymers of opposite helicity that can be easily inverted, in a reversible way, by changing the nature of the anion as revealed by circular dichroism experiments both in solution and in the solid state.

chemistry.chemical_classificationCytidine monophosphateCircular dichroismStereochemistryAbsolute configurationGeneral ChemistryPolymerHelicityPerchloratechemistry.chemical_compoundCrystallographychemistrySelf-assemblyTrifluoromethanesulfonateChemical Science
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Synthesis of cyclic dipeptide templates, their incorporation into peptides and studies on their conformational and biological properties.

2009

This study investigated the diastereoselective synthesis of three dipeptide templates 1, 2 and 3, which may be regarded as conformationally restricted analogs of H-Gly-Xaa-OH, in which Xaa constitutes an aromatic amino acid. Bond formation between α-C of Gly and the aromatic moiety was achieved by proton-catalyzed intramolecular electrophilic aromatic substitution. The absolute configuration of the dipeptide templates was determined by single-crystal X-ray crystallography or by nuclear Overhauser enhancement measurements. A protective group strategy was elaborated to allow their incorporation into peptide sequences by liquid phase as well as by solid-phase peptide synthesis. The templates w…

chemistry.chemical_classificationDipeptideStereochemistryProtein ConformationAbsolute configurationPeptideDermorphinTemplates GeneticElectrophilic aromatic substitutionCrystallography X-RayBiochemistryCombinatorial chemistryPeptides Cyclicchemistry.chemical_compoundStructure-Activity RelationshipEndocrinologychemistryPeptide synthesisAromatic amino acidsIsoquinolineThe journal of peptide research : official journal of the American Peptide Society
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Determination of the absolute configuration of (−)-abietic acidviaits (4R,5R,9R,10R)-7,13-abietadien-18-ylp-bromobenzoate derivative

2006

The absolute configuration of the title bromo derivative of abietic acid, C27H35BrO2, has been determined. The structural analysis confirms the absolute stereochemistry for (−)-abietic acid proposed by Bose & Struck [(1959). Chem. Ind. (London), pp. 1628–1630] on the basis of optical rotatory dispersion measurements. The mol­ecule exhibits a trans anti 6/6/6 tricyclic hydro­carbon skeleton, with the cyclo­hexane ring in the expected chair form and the two cyclo­hexene rings, the double bonds of which are conjugated, in half-chair conformations.

chemistry.chemical_classificationDouble bondAbsolute configurationGeneral ChemistryConjugated systemCondensed Matter PhysicsRing (chemistry)Medicinal chemistrychemistry.chemical_compoundBenzoate derivativechemistryGeneral Materials ScienceAbietic acidOptical rotatory dispersionDerivative (chemistry)Acta Crystallographica Section E Structure Reports Online
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(1S,2R,4S)-1-[(Benzyl­amino)­meth­yl]-4-(prop-1-en-2-yl)cyclo­hexane-1,2-diol

2010

The title compound, C17H25NO2, was synthesized by epoxidation of the double bond of (S)-perillyl alcohol [(S)-4-isopropenyl-1-cyclohexenylmethanol], followed by the oxirane ring-opening by benzylamine using [Ca(CF3CO2)2] as catalyst under solvent-free condition at 313 K. The molecular conformation is stabilized by an intramolecular O—H...N hydrogen bond. In the crystal, molecules are linked by intermolecular N—H...O hydrogen bonds, forming chains parallel to the a axis, which are further connected by O—H...O hydrogen bonds into sheets parallel to (010). The absolute configuration of the molecule is known from the synthetic procedure.

chemistry.chemical_classificationDouble bondHydrogen bondDiolAbsolute configurationAlcoholGeneral ChemistryCondensed Matter PhysicsBioinformaticsMedicinal chemistryOrganic PapersCatalysisHexaneCrystallcsh:Chemistrychemistry.chemical_compoundchemistrylcsh:QD1-999General Materials ScienceActa Crystallographica Section E: Structure Reports Online
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Binding and isomerization energies for the Cu/CN and Cu(I)CN interactions

1993

Abstract Binding and isomerization energies of the CuCN, CuNC, CuCN+, and CuNC+ systems were investigated by means of a multireference CI perturbatively selected, MRCI-PS approach. The inclusion of the main dynamical correlation effects are evaluated. The binding energies for CuCN and CuNC are 4.37 and 4.03 eV, respectively, and those for CuCN+ and CuNC+ are 0.08 and 1.61 eV. Calculated isomerization energies are 7.86 and 35.98 kcal/mol for CuCN and Cu(I)CN isomerizations, respectively.

chemistry.chemical_classificationElectronic correlationBinding energyGaussian orbitalGeneral Physics and AstronomyConfiguration interactionBond-dissociation energyCrystallographychemistryComputational chemistryElectron affinityPhysical and Theoretical ChemistryInorganic compoundIsomerizationChemical Physics
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