Search results for "ether"

showing 10 items of 986 documents

Computational Study of Nanosized Drug Delivery from Cyclodextrins, Crown Ethers and Hyaluronan in Pharmaceutical Formulations

2015

Abstract The problem in this work is the computational characterization of cyclodextrins, crown ethers and hyaluronan (HA) as hosts of inclusion complexes for nanosized drug delivery vehicles in pharmaceutical formulations. The difficulty is addressed through a computational study of some thermodynamic, geometric and topological properties of the hosts. The calculated properties of oligosaccharides of D-glucopyranoses allow these to act as co-solvents of polyanions in water. In crown ethers, the central channel is computed. Mucoadhesive polymer HA in formulations releases drugs in mucosas. Geometric, topological and fractal analyses are carried out with code TOPO. Reference calculations are…

chemistry.chemical_classificationCyclodextrinsMolecular StructureStereochemistryChemistry PharmaceuticalGeneral MedicinePolymerFractal dimensionRelative stabilityNanostructuresMucoadhesive polymersDrug Delivery SystemsFractalchemistryCrown EthersDrug DiscoveryDrug deliveryPhysical chemistryReactivity (chemistry)Hyaluronic AcidParticle SizeHydrate
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pH-Dependent ligands as carriers in transport experiments

2004

Abstract Conformationally pH-regulated ligands have been used as carriers in transport experiments. The experiments were carried out through bulky membranes and the pH at the source phase and at the receiving phase were modified to study the ability of ligands to act as pH-regulated carriers. The influence of pH on transport efficiency seems to be related to its influence on conformational equilibrium. X-ray determination of one precursor compound has been useful for determining the stereochemistry of one of the carriers. To cite this article: A.M. Costero et al., C. R. Chimie 7 (2004).

chemistry.chemical_classificationCyclohexaneStereochemistryGeneral Chemical EngineeringPh dependentGeneral ChemistryCycloalkanechemistry.chemical_compoundMembraneHydrocarbonchemistryComputational chemistryPhase (matter)X-ray crystallographyCrown etherComptes Rendus Chimie
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Screening of ligands for the Ullmann synthesis of electron-rich diaryl ethers

2012

In the search for new ligands for the Ullmann diaryl ether synthesis, permitting the coupling of electron-rich aryl bromides at relatively low temperatures, 56 structurally diverse multidentate ligands were screened in a model system that uses copper iodide in acetonitrile with potassium phosphate as the base. The ligands differed largely in their performance, but no privileged structural class could be identified.

chemistry.chemical_classificationC–O bond formationDenticityBase (chemistry)catalysisArylOrganic Chemistrynucleophilic aromatic substitutiondiaryl ethersUllmann-type couplingCombinatorial chemistryFull Research PaperCatalysislcsh:QD241-441Chemistrychemistry.chemical_compoundchemistrylcsh:Organic chemistryNucleophilic aromatic substitutionPotassium phosphateOrganic chemistrylcsh:QAcetonitrilelcsh:ScienceCopper iodideBeilstein Journal of Organic Chemistry
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A neutral 2D oxalate-based soluble magnet assembled by hydrogen bonding interactions

2008

Abstract Herein we describe the synthesis, structure and magnetic properties of a novel oxalate-based layered magnetic system: {[Mn(OH2)2(S)2][Mn(S)(OH2)]2[Cr(ox)3]2(18-crown-6)}∞ (S = CH3OH; ox = C 2 O 4 2 - ; 18-crown-6 = C12H24O6) (1). In this case, no cationic templating agent is required to promote the assembling of low-dimensional oxalate-bridged metallic complexes in solution. Instead, strong enough hydrogen bonding interactions are responsible for their packing in the solid state. This magnet is soluble and presents two different types of oxalate bridges: the common bis(bidentate) and the unusual bidentate–monodentate. This structural feature has drastic consequences on the magnetis…

chemistry.chemical_classificationDenticityHydrogen bondMagnetismInorganic chemistryCationic polymerizationOxalateInorganic ChemistryMetalchemistry.chemical_compoundCrystallographychemistryFerrimagnetismvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryCrown etherInorganica Chimica Acta
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Carbazole synthesisviaanin situtrapping strategy with indolyl enol ethers

1994

Indolyl enol ethers, generated from the alkoxy(indolyl)carbenium tetra- fluoroborates (1) by treatment with sodium hydride, can be trapped with dimethyl acetylenedicarboxylate or N-phenylmaleimide to furnish the se- lectively functionalized carbazoles (3), (4), (5), (9), (10), and (13). In addition, the biaryl derivatives (6) and (11) are produced by a ring- opening reaction of the primarily formed Diels-Alder adduct. In the case of the biaryl derivative (6), an X-ray crystal structure analysis yields valuable information on constitutions and configurations in the biaryl series. The phenomenon of atropisomerism is discussed for this compound

chemistry.chemical_classificationDimethyl acetylenedicarboxylateAtropisomerCarbazoleOrganic ChemistryEnolMedicinal chemistryAdductSodium hydridechemistry.chemical_compoundchemistryEnol etherAlkoxy groupOrganic chemistryJournal of Heterocyclic Chemistry
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Diorganotin(IV) dipeptide complexes with potential antitumour activity

1993

A series of complexes of the dimethylltin(IV) moiety with dipeptides has been synthesized. The dipeptides are L-alanyl-L-histidine (H2AlaHis), L-methionyl-L-methionine (H2MetMet), L-glycyl-L-histidine (H2GlyHis) and L-histidyl-L-glycine (H2HisGly). The complexes have been characterized by IR and 119Sn Mossbauer spectroscopy in the solid state and by 1H NMR in CD3OD and D2O solutions. They consist of monomeric entities, with the tin atom arranged in a pentacoordinated trigonal bipyramidal structure. The dipeptides are coordinated via the amino group, deprotonated peptide nitrogen and carboxylate group. Neither imidazole in histidine-containing dipetides, nor the thioether group in MetMet, is…

chemistry.chemical_classificationDipeptideChemistryStereochemistryPeptideGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometryThioetherMoietyImidazoleCarboxylateApplied Organometallic Chemistry
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Methyl 3-(4-methoxyphenyl)prop-2-enoate

2001

The title molecule, C(11)H(12)O(3), is almost planar, with an average deviation of the C and O atoms from the least-squares plane of 0.146(4)A. The geometry about the C=C bond is trans. The phenyl ring and -COOCH(3) group are twisted with respect to the double bond by 9.3(3) and 5.6(5) degree, respectively. The endocyclic angle at the junction of the propenoate group and the phenyl ring is decreased from 120 degree by 2.6(2) degree, whereas two neighbouring angles around the ring are increased by 2.3(2) and 0.9(2) degree. This is probably associated with the charge-transfer interaction of the phenyl ring and -COOCH(3) group through the C=C double bond. The molecules are joined together thro…

chemistry.chemical_classificationDouble bondHydrogen bondStereochemistryEtherGeneral MedicineCrystal structureRing (chemistry)General Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundCrystallographychemistryZigzagGroup (periodic table)MoleculeActa Crystallographica Section C-Crystal Structure Communications
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ChemInform Abstract: Stereoselective Synthesis of 7,11-Guaien-8,12-olides from Santonin. Synthesis of Podoandin and (+)-Zedolactone A.

2001

Photochemical rearrangement of hydroxy ester 2, easily obtained from santonin (1), afforded butenolide 4, a good starting material for the synthesis of 7,11-guaien-8,12-olides. Compound 4 has been transformed into compound 10, which has been used for the synthesis of podoandin (5) and (+)-zedolactone A (ent-6). Regioselective elimination of the acetyl group on C10 afforded directly podoandin (5). For the synthesis of ent-6, a hydroxyl group has been regio- and stereoselectively introduced at the 4α-position through the 3α,4α-epoxide 15. The basic hydrolysis of the 10-acetyl group in compound 18 took place with concomitant intramolecular conjugated addition of the alkoxide to the butenolide …

chemistry.chemical_classificationElimination reactionchemistry.chemical_compoundChemistryStereochemistryMoietyRegioselectivityEtherStereoselectivityGeneral MedicineEnantiomerLactoneButenolideChemInform
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Efficiency Boosting of Surfactants with Poly(ethylene oxide)-Poly(alkyl glycidyl ether)s: A New Class of Amphiphilic Polymers

2020

Twenty years ago, it was found that adding small amounts of amphiphilic block copolymers like poly(ethylene propylene)-co-poly(ethylene oxide) (PEP-b-PEO) to microemulsion systems strongly increases the efficiency of medium-chain surfactants to solubilize water and oil. Although being predestined to serve as a milestone in microemulsion research, the effect has only scarcely found its way into applications. In this work, we propose new types of efficiency boosters, namely, poly(ethylene oxide)-poly(alkyl glycidyl ether carbonate)s (PEO-b-PAlkGE) and their "carbonated" poly(ethylene oxide)-poly(carbonate alkyl glycidyl ether) analogs. Their synthesis via anionic ring-opening polymerization (…

chemistry.chemical_classificationEthylene oxideEther02 engineering and technologySurfaces and InterfacesPolymer010402 general chemistry021001 nanoscience & nanotechnologyCondensed Matter Physics01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryPolymerizationChemical engineeringAmphiphileddc:540ElectrochemistryGeneral Materials ScienceMicroemulsion0210 nano-technologyEthylene glycolSpectroscopyAlkyl
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Understanding the affinity of bis-exTTF macrocyclic receptors towards fullerene recognition

2019

A new series of fullerene receptors based on exTTF macrocycles with alkyl ether chains of increasing length is reported. The novel macrocyclic receptors are able to favourably interact with fullerene C60 through a synergistic combination of π–π, CH⋯π and n⋯π noncovalent interactions. We identify that the highest affinity towards C60 recognition is achieved for the host with the tightest fit; that is, the smallest receptor with a cavity large enough to host the buckyball inside (log Ka = 5.2 in chlorobenzene at 298 K). However, besides this expected observation, theoretical calculations evidence that the most stable self-assembling configuration corresponds for all the receptors to an outsid…

chemistry.chemical_classificationFullereneGeneral Physics and Astronomy02 engineering and technologySynergistic combination010402 general chemistry021001 nanoscience & nanotechnology01 natural sciences3. Good health0104 chemical sciencesAlkyl etherchemistry.chemical_compoundCrystallographychemistryChlorobenzeneNon-covalent interactionsPhysical and Theoretical Chemistry0210 nano-technologyReceptorPhysical Chemistry Chemical Physics
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