Search results for "derivati"

showing 10 items of 1360 documents

How amino and nitro substituents affect the aromaticity of benzene ring

2020

Abstract The effect of strongly electron-accepting and electron-donating substituents on the aromaticity of the benzene ring has been revealed based on experimental and computational data. It has been documented that the nitro group affects the π-electron structure of the ring in its benzene derivative ca. 2.8 times weaker than the amino group. However, their joint effects in the meta and para nitroaniline, compared to nitrobenzene, results in a decrease of the delocalization in the ring by a factor ca. 4.0 and 6.5, respectively.

General Physics and AstronomyAromaticity02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPara-nitroanilineRing (chemistry)01 natural sciencesMedicinal chemistry0104 chemical sciencesNitrobenzenechemistry.chemical_compoundDelocalized electronchemistryBenzene derivativesNitroPhysical and Theoretical Chemistry0210 nano-technologyBenzeneChemical Physics Letters
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Squaric Acid Mediated Synthesis and Biological Activity of a Library of Linear and Hyperbranched Poly(Glycerol)-Protein Conjugates

2012

Polymer-protein conjugates generated from side chain functional synthetic polymers are attractive because they can be easily further modified with, for example, labeling groups or targeting ligands. The residue specific modification of proteins with side chain functional synthetic polymers using the traditional coupling strategies may be compromised due to the nonorthogonality of the side-chain and chain-end functional groups of the synthetic polymer, which may lead to side reactions. This study explores the feasibility of the squaric acid diethyl ester mediated coupling as an amine selective, hydroxyl tolerant, and hydrolysis insensitive route for the preparation of side-chain functional, …

GlycerolModels MolecularCovalent AttachmentPolymers and PlasticsPolymersBioengineeringSquaric acidImmunological PropertiesLigandsSmall Molecule LibrariesBiomaterialsHydrolysischemistry.chemical_compoundResidue (chemistry)Thiazolidine-2-ThioneMaterials ChemistrySide chainCopolymerOrganic chemistryBovine Serum-Albuminchemistry.chemical_classificationPoly(Ethylene Glycol)Molecular StructureCopolymersPolymer StructureSerum Albumin BovinePolymerPolyethylene-GlycolMolecular WeightPolyglycerolschemistryMuramidaseAmine gas treatingFunctional polymersCyclobutanesDerivatives
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Beyond Poly(ethylene glycol): Linear Polyglycerol as a Multifunctional Polyether for Biomedical and Pharmaceutical Applications

2014

Polyglycerols (sometimes also called "polyglycidols") represent a class of highly biocompatible and multihydroxy-functional polymers that may be considered as a multifunctional analogue of poly(ethylene glycol) (PEG). Various architectures based on a polyglycerol scaffold are feasible depending on the monomer employed. While polymerization of glycidol leads to hyperbranched polyglycerols, the precisely defined linear analogue is obtained by using suitably protected glycidol as a monomer, followed by removal of the protective group in a postpolymerization step. This review summarizes the properties and synthetic approaches toward linear polyglycerols (linPG), which are at present mainly base…

Glycerolchemistry.chemical_classificationPolymers and PlasticsPolymersGlycidolBiocompatible MaterialsBioengineeringPolymerPolyethylene GlycolsBiomaterialschemistry.chemical_compoundMonomerPharmaceutical PreparationschemistryPolymerizationPEG ratioMaterials ChemistryAnimalsHumansSurface modificationOrganic chemistryEthylene glycolDerivative (chemistry)EthersBiomacromolecules
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In syringe hybrid monoliths modified with gold nanoparticles for selective extraction of glutathione in biological fluids prior to its determination …

2020

Abstract In this work, a simple device for extraction glutathione (GSH) in biological fluids using a hybrid monolithic material within a polypropylene syringe is developed. For this purpose, glycidyl methacrylate-based monolith was firstly prepared within this housing material, and the polymer was modified with different ligands (ammonia, cysteamine and cystamine). The resulting materials (containing amine or thiol groups, respectively) were then functionalized with gold nanoparticles (AuNPs). The hybrid material that gave the largest AuNPs coverage was selected as solid-phase (SPE) sorbent and several variables affecting the extraction recovery of this compound were investigated. Under opt…

Glycidyl methacrylateMetal Nanoparticles02 engineering and technology01 natural sciencesAnalytical Chemistrychemistry.chemical_compoundLimit of DetectionHumansSolid phase extractionMonolithDerivatizationSalivaChromatography High Pressure LiquidDetection limitgeographygeography.geographical_feature_categoryChromatographySyringes010401 analytical chemistryExtraction (chemistry)Solid Phase ExtractionReproducibility of Results021001 nanoscience & nanotechnologyGlutathione0104 chemical scienceschemistryColloidal goldEpoxy CompoundsMethacrylatesGold0210 nano-technologyHybrid materialTalanta
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Fractal geometry of higher derivative gravity

2019

We determine the scaling properties of geometric operators such as lengths, areas, and volumes in models of higher derivative quantum gravity by renormalizing appropriate composite operators. We use these results to deduce the fractal dimensions of such hypersurfaces embedded in a quantum spacetime at very small distances.

Gravity (chemistry)geometryoperator: geometricalGeneral Physics and AstronomyFOS: Physical sciencesGeneral Relativity and Quantum Cosmology (gr-qc)derivative: highQuantum spacetimeGravitation and Astrophysics01 natural sciencesFractal dimensionGeneral Relativity and Quantum CosmologyGravitationGeneral Relativity and Quantum CosmologyFractal0103 physical sciencesfractal: dimension010306 general physicsScalingEffective actionPhysicsMathematical analysisscalingtensor: Weylsymmetry: Weyleffective actionspace-timequantum gravitygravitation[PHYS.GRQC]Physics [physics]/General Relativity and Quantum Cosmology [gr-qc]Quantum gravityoperator: composite
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A Bipyridine‐Palladium Derivative as General Pre‐Catalyst for Cross‐Coupling Reactions in Deep Eutectic Solvents

2019

A versatile and DES‐compatible bipyridine palladium complex has been developed as a general pre‐catalyst for different cross‐coupling reactions (Hiyama, Suzuki‐Miyaura, Heck‐Mizoroki and Sonogashira) in deep eutectic solvents. Hydrogen bond capacity of the ligand allows to keep the excellent level of results previously obtained in classical organic solvents. Palladium pre‐catalyst showed a high catalytic activity for many cross‐coupling reactions, demonstrating a great versatility and applicability. Also, this methodology employs sustainable solvents as a reaction medium and highlights the potential of DES as alternative solvents in organometallic catalysis. The catalyst and DES were easily…

Green chemistry010405 organic chemistryHydrogen bondchemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCoupling reaction0104 chemical sciencesCatalysisHydrogen bondsLigand designchemistry.chemical_compoundBipyridineQuímica OrgánicachemistryGreen chemistryPolymer chemistryCross-couplingDerivative (chemistry)PalladiumEutectic systemPalladium
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Efficient microwave-assisted synthesis of glycerol monodecanoate

2017

International audience; Solvent-free microwave-assisted synthesis was carried out to prepare 2,3-dihydroxypropyl decanoate, by esterification of decanoic acid in the presence of two distinct glycerol derivatives, glycidol, and glycerol carbonate, respectively. The process described is based on microwaves heating source with electrical power in the range of 200–400 W, involving stoichiometric proportions of decanoic acid and glycerol derivatives, and using catalytic amounts of TBAI used as organocatalyst. Conversion and selectivity rates of esterification reactions were monitored by 1H and 13C{1H} NMR spectroscopy. The predominantly formed ester, 2,3-dihydroxypropyl decanoate was fully chara…

Green chemistryBio-based building-blocksGlycerol derivatives02 engineering and technology010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundGlycerolOrganic chemistry[CHIM]Chemical Sciences1-MonoacylglycerolComputingMilieux_MISCELLANEOUSGlycidolGeneral ChemistryDecanoic acidNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesMicrowave-assisted organic chemistrychemistryGreen chemistry13. Climate action0210 nano-technologySelectivityStoichiometryFood ScienceBiotechnology
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Imidazolium and Potassium Hydrogen Carbonate Salts as Ecofriendly Organocatalysts for Oxazolidinone Synthesis

2016

International audience; Although oxazolidinones are valuable intermediate compounds for industrial applications, no synthetic method is suitable for their production on a large scale owing to the use of reagents/catalysts that are hazardous or toxic to human health or ecotoxic for the environment. In this manuscript, we describe new and efficient catalysts, that is, the nontoxic hydrogen carbonate anion in combination with a potassium or diisobutylimidazolium ([iBu(2)IM]) countercation, for the conversion of -amino alcohols into cyclic oxazolidinones in high yields of 69 to 90%. Depending on the catalytic conditions, both catalysts could be easily recovered from the crude reaction products …

Green chemistryHydrogenPotassiumchemistry.chemical_elementHomogeneous catalysisantibacterial agentsHeterocyclesamino-alcohols010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencescatalystsCatalysisefficientchemistry.chemical_compounddioxide[ CHIM.ORGA ] Chemical Sciences/Organic chemistryOrganic chemistry[CHIM]Chemical SciencesSustainable chemistryPhysical and Theoretical ChemistryComputingMilieux_MISCELLANEOUS010405 organic chemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganocatalysisOrganic Chemistry[CHIM.CATA]Chemical Sciences/CatalysisHomogeneous catalysis0104 chemical scienceschemistryCyclizationOrganocatalysisReagentderivativesCarbonateacid
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Undecylenic acid: A tunable bio-based synthon for materials applications

2016

International audience; An undecylenic acid-based monoglyceride prepared from glycidol and undecylenic acid is used as suitable and tunable synthon for polymerization applications. Epoxidation and acrylation reactions lead to photopolymerizable monomers while transesterification with dimethyl carbonate, metathesis and aminolysis reactions provide access to polyhydroxyurethane-based materials. The successive intermediates were synthesized according to a green chemistry approach implicating solvent-less and catalyzed reactions, and were at each step fully characterized by infrared, 1H and 13C{1H} NMR spectroscopy, elemental analysis and mass spectrometry. Analyses of the resulting polymer mat…

Green chemistryThermogravimetric analysisRenewable resourcesMaterials sciencePolymers and PlasticsOrganic carbonatepolyhydroxyurethanespolyurethanesGeneral Physics and Astronomy02 engineering and technologycyclic carbonates010402 general chemistry01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundPolyhydroxyurethanes (PHUs)Aminolysisrenewable building-blockPolymer chemistryMaterials ChemistrymedicineOrganic chemistry[CHIM]Chemical Sciencessolvent-free conditionscastor-oilglycerol carbonatePhotopolymerizationOrganic ChemistrySynthonGlycidolTransesterification021001 nanoscience & nanotechnologyFatty acid0104 chemical scienceschemistryPolymerizationGlycidolpolycarbonatespolymerizationUndecylenic acidderivatives0210 nano-technologymedicine.drug
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One-Pot Synthesis of Polysubstituted Pyrrolidines from Aminonitriles

2005

α-Aminonitriles with a mono- or unsubstituted amino group as well as a-(alkylideneamino)nitriles can be employed as easily accessible α-aminocarbanion equivalents. Their α-deprotonation yields stabilized carbanions, whichundergo smooth 1,4-addition to α,β-unsaturated carbonyl compounds. The resulting δ-ketoα-aminonitriles can be reductively cyclized to form polysubstituted pyrrolidines.

Group (periodic table)ChemistryOrganic ChemistryOne-pot synthesisOrganic chemistryGeneral MedicinePyrrole derivativesCatalysisCarbanionSynthesis
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