Search results for "ALK"

showing 10 items of 4314 documents

Semisynthesis of new tetrahydrofuranic alkyl ester and furano-pyrone derivatives as inhibitors of the mitochondrial complex I

2002

Abstract Methoxymethylation of altholactone ( 1 ) led to the corresponding O -methoxymethyl derivative ( 3 ) in addition to the unexpected 6,7-dihydro-7-methoxy analogue ( 4 ), and two original tetrahydrofuranic (THF) alkyl esters ( 5 , 6 ). Moreover, when we accomplished a new method for the preparation of the furano-pyrone goniofupyrone ( 7 ) through 7-hydroxylation of 1 in acid medium, a minor compound ( 8 ) with an identical skeleton to that of compounds 5 and 6 was identified. Careful examination of the published spectral data of the reported styryl-lactones with an heptolide skeleton reveals that those structures possess also a THF alkyl ester skeleton. The revision of those structure…

chemistry.chemical_classificationAltholactoneStereochemistryOrganic ChemistryBiochemistrySemisynthesisChemical correlationPyroneGoniofupyronechemistry.chemical_compoundchemistryDrug DiscoverySpectral dataAlkylMitochondrial Complex ITetrahedron
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Photochemical versus aluminium chloride-catalyzed fries rearrangement of aryl hydrogen succinates. synthesis of 2(3H)-furanones

1989

The photochemical and aluminium chloride-catalyzed Fries rearrangement of a series of aryl hydrogen succinates3 a–f to the corresponding 4-oxoacids1 a–f are compared. Both approaches are complementary: the photochemical process is more general and becomes the method of choice for the succinoylation of phenols supporting alkoxy or hydroxy substituents, while the classical rearrangement is superior in the presence of alkyl or halogen substituents. These results are applied to the preparation of the 2(3H)-furanones2 a–f.

chemistry.chemical_classificationAluminium chlorideFries rearrangementArylGeneral ChemistryPhotochemistryCatalysischemistry.chemical_compoundchemistryHalogenSuccinatesAlkoxy groupmedicineOrganic chemistryAlkylmedicine.drugMonatshefte f�r Chemie Chemical Monthly
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Comparison of an indirect format ELISA on modified graphite and polystyrene surfaces against triazines.

2006

An indirect format enzyme-linked immuno-sorbent assay (ELISA) on graphite rods (Ø 0.8 mm x 20 mm) and, for comparison, on microtiter plates has been developed against terbuthylazine. For this purpose, a series of 2-aminoalkyl-4-chloro-6-terbuthyl-s-triazine-2,6- diamine ELISA haptens with alkyl spacer lengths of 2, 4, 6, and 8 CH2 groups has been synthesized. The graphite rods or the microtiter plates were covered by a polymerized glutaraldehyde network, and the ELISA haptens have been coupled by imino coupling to the free aldehyde groups of that network. ε-Aminocaproic acid has been used as an agent to block unspecific binding sites. The ELISA was run in a competitive mode, where the immob…

chemistry.chemical_classificationAnalyteChromatographySurface PropertiesTriazinesEnzyme-Linked Immunosorbent AssayTerbuthylazineAldehydeGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundchemistryPolystyrenesGraphiteGraphitePolystyreneGlutaraldehydeHaptenHaptensAlkylZeitschrift fur Naturforschung. C, Journal of biosciences
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Synthesis of Lamellarin D Trimethyl Ether and Lamellarin H via 6π-Electrocyclization.

2015

An electrocyclic ring closure of a 2-azapentadienyl anion generated in situ from a chalcone and glycine ester is the key step of an efficient synthesis of the pyrrole core of the lamellarin alkaloids. A recently developed scalable one-pot procedure provides multigram quantities of a 3,5-diaryl-4-iodopyrrole-2-carboxylate intermediate which is transformed in four further high-yielding operations including a one-pot Pomeranz–Fritsch alkylation/cyclization and an Ullmann-type lactone ring closure into the pentacyclic lamellarin skeleton.

chemistry.chemical_classificationAnionsChalconeAlkylationMolecular StructureStereochemistryOrganic ChemistryEtherStereoisomerismStereoisomerismAlkylationRing (chemistry)IsoquinolinesHeterocyclic Compounds 4 or More Ringschemistry.chemical_compoundchemistryCoumarinsCyclizationLamellarin DPyrrolesLactonePyrroleEthersThe Journal of organic chemistry
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A novel synthesis of polymers with anthracene and dihydroanthracene subunits in the main chain

1993

A new polycondensation method to connect redox-active and chromophoric subunits by forming a C-C bond and leading to a polyhydrocarbon is described. 1,ω-bis(9,10-Dihydro-9-anthry)alkanes with various alkylene spacers can be deprotonated by butyllithium to afford a monoanion in each dihydroanthracene moiety. Alkylation with dielectrophiles such as dibromoalkanes yields soluble polymers with dihydroanthracene units in the main chain. The reaction proceeds regioselectively in the 9,10-position. Aromatization generates a polymer with anthracene units. The molecular weights are determined by GPC up to Mn = 10 000. To prove the structure and to calibrate the GPC, suitable model compounds were syn…

chemistry.chemical_classificationAnthraceneCondensation polymerPolymers and PlasticsOrganic ChemistryAromatizationPolymerAlkylationchemistry.chemical_compoundDeprotonationchemistryPolymer chemistryMaterials ChemistryButyllithiumMoietyPolymer International
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Anthracene Based Conjugated Polymers: Correlation between π−π-Stacking Ability, Photophysical Properties, Charge Carrier Mobility, and Photovoltaic P…

2010

This article reports on the synthesis, characterization and properties of a series of anthracene−containing poly(p-phenylene-ethynylene)-alt-poly(p-phenylene-vinylene)s (PPE−PPV) copolymers with general constitutional unit (Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n denoted AnE-PV. Solely linear (AnE-PVaa, -ad, -ae) and solely branched (AnE-PVbb) as well as mixed linear and branched (AnE-PVab, -ac, -ba, -cc) alkoxy side chains were grafted to the backbone in order to tune the π−π-stacking ability of the materials. It has been possible to establish a correlation between π−π-stacking ability, absorptive behavior, charge carrier mobility, solar cell active layer nanoscale morphology and resulting p…

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsOpen-circuit voltageOrganic ChemistryStackingPolymerConjugated systemlaw.inventionInorganic Chemistrychemistry.chemical_compoundCrystallographychemistrylawSolar cellPolymer chemistryMaterials ChemistrySide chainAlkoxy groupMacromolecules
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Intercorrelation between Structural Ordering and Emission Properties in Photoconducting Polymers

2009

We investigated the structural properties of anthracene containing poly(p-phenylene−ethynylene)-alt-poly(p-phenylene−vinylene) polymers with general constitutional unit: (−Ph−C≡C−Anthr−C≡C−Ph−CH═CH−Ph−CH═CH−)n by means of wide-angle X-ray scattering and fluorescence spectroscopy. Interchain interactions were systematically modified by decorating the conjugated polymer backbone with linear or branched or combinations of linear and branched alkoxy side chains. Special emphasis is taken on an evaluation method for fiber scattering spectra that allows the deduction of important structural details of polymer materials with limited degree of order. These include positional correlations along the …

chemistry.chemical_classificationAnthraceneMaterials sciencePolymers and PlasticsScatteringOrganic ChemistryStackingPolymerConjugated systemFluorescence spectroscopyInorganic ChemistryCrystallographychemistry.chemical_compoundchemistryPolymer chemistryMaterials ChemistryAlkoxy groupSide chainMacromolecules
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Oxygen atom transfer catalysis by dioxidomolybdenum(VI) complexes of pyridyl aminophenolate ligands

2021

Abstract A series of new cationic dioxidomolybdenum(VI) complexes [MoO2(Ln)]PF6 (2–5) with the tripodal tetradentate pyridyl aminophenolate ligands HL2-HL5 have been synthesized and characterized. Ligands HL2-HL4 carry substituents in the 4-position of the phenolate ring, viz. Cl, Br and NO2, respectively, whereas the ligand HL5, N-(2-hydroxy-3,5-di-tert-butylbenzyl)-N,N-bis(2-pyridylmethyl)amine, is a derivative of 3,5-di-tert-butylsalicylaldehyde. X-ray crystal structures of complexes 2, 3 and 5 reveal that they have a distorted octahedral geometry with the bonding parameters around the metal centres being practically similar. Stoichiometric oxygen atom transfer (OAT) properties of 5 with…

chemistry.chemical_classificationAqueous solution010405 organic chemistryChemistryLigandAlkeneDimerCationic polymerization010402 general chemistry01 natural sciences0104 chemical sciencesCatalysisInorganic Chemistrychemistry.chemical_compoundOctahedral molecular geometryPolymer chemistryMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryPolyhedron
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The Catalytic Effect of Fluoroalcohol Mixtures Depends on Domain Formation

2017

In the present contribution, we investigated catalytically active mixtures of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and aqueous H2O2 by molecular dynamics simulations. It is clearly observable that the HFIP molecule strongly binds to the H2O2, which is necessary for the desired catalytic reaction to occur. Upon the addition of the substrate cyclooctene to the solution, this interaction is enhanced, which suggests that the catalytic activity is increased by the presence of the hydrocarbon. We could clearly observe the microheterogeneous structure of the mixture, which is the result of the separation of the hydroxyl groups, water, and H2O2 from the fluorinated alkyl moiety in the form of l…

chemistry.chemical_classificationAqueous solution010405 organic chemistrySubstrate (chemistry)General Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundHydrocarbonchemistryCycloocteneMoietyOrganic chemistryMoleculeAlkylACS Catalysis
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Self-assembly properties of bile acid derivatives of L-cysteine, L-valine and L-serine alkyl esters

2012

Comprehensive self-assembly studies for nine bile acid amides of amino acid esters are reported. The number of the hydroxyl groups attached to the steroidal skeleton and the character of the amino acid ester moiety were used as variables when examining the self-assembly properties of the compounds. Two of the compounds were shown to undergo self-assembly leading to organogelation. In addition, preliminary self-assembly studies in aqueous mixtures of polar organic solvents were conducted. Microscopic methods (optical microscopy and scanning electron microscopy) were utilised in order to gain a deeper insight into the self-assembled structures. Furthermore, single-crystal X-ray structures for…

chemistry.chemical_classificationAqueous solutionBile acidmedicine.drug_classStereochemistryGeneral ChemistryAmino acidchemistryValineX-ray crystallographymedicineOrganic chemistryMoietySelf-assemblyta116AlkylSupramolecular Chemistry
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