Search results for "Esters"

showing 10 items of 305 documents

Method for evaluating the bioconversion of radioactive polyunsaturated fatty acids by use of reversed-phase liquid chromatography

1988

Abstract Reversed-phase high-performance liquid chromatography on a thermostatted octadecylsilyl column was used to separate mixtures of labelled polyunsaturated fatty acids (as their methyl esters) formed by successive desaturations and elongations of labelled linoleic (18:2 n - 6) or linolenic (18:3 n -3) acid by rat liver microsomes. Acetonitrile-water mixtures were used for elution of the esters. Unsaturated and saturated esters were detected by their refractive indices. The order of elution of fatty acid methyl esters in complex mixtures varies as a function of the chain length and unsaturation, analysis temperature, water concentration and solvent flow-rate. The peak areas vary as a f…

chemistry.chemical_classificationDegree of unsaturationChromatography GasChromatographyElutionChemistryOrganic ChemistryTemperatureFatty acidEstersGeneral MedicineReversed-phase chromatographyMetabolismFatty Acids NonesterifiedBiochemistryHigh-performance liquid chromatographyAnalytical ChemistrySolventsUnsaturated fatty acidChromatography LiquidPolyunsaturated fatty acidJournal of Chromatography A
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o-Boronato- and o-Trifluoroborato-Phosphonium Salts Supported by L-α-Amino Acid Side Chain.

2015

The synthesis of o-boronato- and o-trifluoroborato-phosphonium salts supported by the L-amino acid side chain is described. The synthesis of these new class of amino acid derivatives was achieved by stereoselective quaternization of o-(pinacolato)boronatophenylphosphine with β- or γ-iodo amino acid derivatives which are prepared from L-serine or L-aspartic acid, respectively. The quaternization of the phosphine was performed using either iodo amino ester or carboxylic acid derivatives. In addition, free carboxylic acid and amine derivatives were obtained by saponification or HCl acidolysis of o-boronato-phosphonium amino esters, respectively. The usefulness of these compounds in peptide cou…

chemistry.chemical_classificationDipeptideAmino estersMolecular StructureChemistryCarboxylic acidOrganic ChemistryAmino acidchemistry.chemical_compoundHydrolysisOrganophosphorus CompoundsAspartic acidBoratesSide chainOrganic chemistrySaltsPhosphoniumAmino AcidsThe Journal of organic chemistry
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Modular Hemisyntheses of Boronato- and Trifluoroborato-SubstitutedL-NHBoc Amino Acid and Peptide Derivatives

2013

Modular hemisyntheses of boronato- and trifluoroborato-substituted amino acid and peptide derivatives by using Wittig and C–H iridium-catalyzed borylation as key reactions, are described. Amino ester precursors bearing an aromatic moiety on a lateral chain were prepared by reaction of a new L-NHBoc-amino acid Wittig reagent with the corresponding aromatic aldehydes. After esterification and hydrogenation, the borylation of amino esters was achieved with yields up to 82 % by using the catalysed reaction of bis(pinacolato) diborane reagent (B2Pin2) in the presence of an iridium complex. Interestingly, this iridium-catalyzed borylation was also performed with a dipeptide in 78 % yield. Finally…

chemistry.chemical_classificationDipeptideAmino estersOrganic ChemistryPeptideBorylationCombinatorial chemistryAmino acidHydrolysischemistry.chemical_compoundchemistryReagentWittig reactionPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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A Deeper Insight into the Postpolymerization Modification of Polypenta Fluorophenyl Methacrylates to Poly(N -(2-Hydroxypropyl) Methacrylamide)

2014

This work provides a detailed insight into the synthesis of N-(2-hydroxypropyl)methacrylamide (HPMA) polymers employing the activated ester approach. In this approach, polypenta fluorophenyl methacrylate (PFPMA)-activated ester polymers are synthesized by the reversible addition-fragmentation chain transfer (RAFT) polymerization and transferred into HPMA-based systems by the use of 2-hydroxypropylamine. To prove quantitative conversion in the absence of side reactions, special attention is devoted to investigate different reaction conditions by different analytical methods ((1) H, (19) F, inverse-gated (13) C NMR, and zeta potential measurements). Furthermore the influence of common solvent…

chemistry.chemical_classificationMagnetic Resonance SpectroscopyMaterials sciencePolymers and PlasticsPolymersHydrolysisOrganic ChemistryWaterEstersChain transferPolymerMethacrylatePolymerizationKineticschemistry.chemical_compoundPolymethacrylic AcidsPolymerizationchemistryTacticityPolymer chemistryMaterials ChemistryZeta potentialOrganic chemistryMethacrylamideN-(2-Hydroxypropyl) methacrylamideMacromolecular Rapid Communications
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Reactive nanorods based on activated esterpolymers: a versatile template-assisted approach for the fabrication of functional nanorods

2011

A new route for the fabrication of polymeric nanorods with functional moieties via post-modification of reactive nanorods is described. To this end reactive nanorods with a homogenous and narrow size distribution were fabricated by utilizing an anodic aluminium oxide (AAO) template-assisted approach. The nanorods are based on activated pentafluorophenyl esters, to enable quantitative post-modification with amines under very mild reaction conditions yielding the corresponding functionalized amide. Post-modification with fluorescent dyes as well as the conversion into well-dispersed rod-shaped poly(N-isopropylacrylamide) (PNIPAM) hydrogels that exhibit a thermal-responsive phase transition wa…

chemistry.chemical_classificationMaterials scienceFabricationPolymers and PlasticsOrganic Chemistrytechnology industry and agricultureBioengineeringNanotechnologyPentafluorophenyl estersPolymerBiochemistrychemistry.chemical_compoundchemistryAmideSelf-healing hydrogelsDrug deliveryAluminium oxideNanorodPolym. Chem.
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On the compatibilization of PET/HDPE blends through a new class of copolyesters

2000

Polyethyleneterephthalate (PET) and polyethylene are incompatible polymers and their blends show, in general, poor properties. Compatibilization is then a necessary step to obtain blends with good mechanical and barrier properties. In this work different compatibilizing agents were used, i.e. a maleic anhydride elastomer and some new products containing graft-copolymers having polyester segments grafted onto polyethylene backbone chains. Both the functionalized elastomer and the new products drastically improve the morphology and the ductility of the blend. In the case of the modified elastomer the compatibilizing action has been attributed to the formation of H-bonds whereas the copolymers…

chemistry.chemical_classificationPOLYETHYLENEMaterials sciencecompatibilizationPolymers and PlasticsOrganic ChemistryPET/HDPE blendsMaleic anhydridePolymerCompatibilizationPolyethyleneElastomercopolyestersLIQUID-CRYSTALLINE POLYMERPolyesterchemistry.chemical_compoundPET/HDPE blends; copolyesters; compatibilization; LIQUID-CRYSTALLINE POLYMER; POLYETHYLENEchemistryChemical engineeringMaterials ChemistryPolymer blendHigh-density polyethyleneComposite materialPolymer
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Synthesis of fluorinated Thomsen-Friedenreich antigens: direct deoxyfluorination of αGalNAc-threonine tert-butyl esters.

2011

Selectively 6-fluorinated analogs of the tumor-associated T(N) antigen Fmoc-Thr(α-O-GalNAc)-OtBu can be efficiently prepared using DAST-mediated de(hydr)oxyfluorination reactions of preformed and orthogonally protected glycosyl amino esters without affecting the labile protecting groups and O-glycosidic linkages. The resulting mono- and difluorinated T(N) analogs are interesting building blocks for non-hydrolyzable mucin-type antigen mimetics, as illustrated by the unprecedented synthesis of two different multiply fluorinated Thomsen-Friedenreich derivatives. The reported deoxyfluoro antigen analogs represent important functional probes for carbohydrate-binding proteins and glycosyl-process…

chemistry.chemical_classificationTert butylThreonineAcetylgalactosamineAmino estersCarbohydrate chemistryStereochemistryOrganic ChemistryFluorineBiochemistrychemistry.chemical_compoundEnzymechemistryAntigenGlycosylAntigens Tumor-Associated CarbohydratePhysical and Theoretical ChemistryThreonineFluorescent DyesOrganicbiomolecular chemistry
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ChemInform Abstract: O-Boronato- and o-Trifluoroborato-Phosphonium Salts Supported by L-α-Amino Acid Side Chain.

2015

The synthesis of o-boronato- and o-trifluoroborato–phosphonium salts supported by the l-amino acid side chain is described. The synthesis of these new class of amino acid derivatives was achieved by stereoselective quaternization of o-(pinacolato)boronatophenylphosphine with β- or γ-iodo amino acid derivatives which are prepared from l-serine or l-aspartic acid, respectively. The quaternization of the phosphine was performed using either iodo amino ester or carboxylic acid derivatives. In addition, free carboxylic acid and amine derivatives were obtained by saponification or HCl acidolysis of o-boronato–phosphonium amino esters, respectively. The usefulness of these compounds in peptide cou…

chemistry.chemical_classificationchemistry.chemical_compoundHydrolysisDipeptideAmino esterschemistryCarboxylic acidAspartic acidSide chainGeneral MedicinePhosphoniumMedicinal chemistryAmino acidChemInform
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ChemInform Abstract: Differential Reactivity of Fluorinated Homopropargylic Amino Esters vs Gold(I) Salts. The Role of the Nitrogen Protecting Group.

2015

The gold(I)-catalyzed hydroarylation/isomerization reaction of N-protected homopropargyl amino esters (III) gives quinoline derivatives of type (IV).

chemistry.chemical_compoundAmino esterschemistryQuinolineOrganic chemistrychemistry.chemical_elementReactivity (chemistry)General MedicineProtecting groupNitrogenIsomerizationChemInform
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Der einfluß benachbarter grundbausteine auf die ammonolyse von essigsäureestern phenolischer mehrkernverbindungen

1972

Die Ammonolyse der Essigsaureester verschiedener phenolischer Zwei- und Dreikernverbindungen, die neben Methylphenolbausteinen jeweils einen Nitrophenolbaustein enthalten, wurde untersucht. In allen Fallen wird wie bei einkernigen Nitrophenylestern die Esterbindung im Nitrophenolbaustein ammonolytisch gespalten. Wenn die Bausteine uber Methylenbrucken in ortho-Stellung zu den phenolischen Hydroxylgruppen verknupft sind, werden jedoch auch die Esterbindungen in den Methylphenolbausteinen gespalten, obwohl die Ester von Methylphenolen und Mehrkernverbindungen, die nur Methylgruppen als Substituenten tragen, unter gleichen Bedingungen durch Ammoniak nicht angegriffen werden. In ubereinstimmung…

chemistry.chemical_compoundAmmoniaNitrophenolchemistryNucleophileStereochemistryPolymer chemistryAcetic Acid EstersMethyleneRate-determining stepDie Makromolekulare Chemie
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