Search results for "Cycloaddition"

showing 10 items of 392 documents

Synthesis, molecular structure and stability of fused bicyclic Δ4-1,2,4-oxadiazoline Pt(II) complexes

2015

Abstract The reaction of trans -[PtCl 2 (NCR) 2 ] (R 1  = CH 2 CO 2 Me ( 1a ), R 2  = CH 2 Cl ( 1b )) with pyrroline N -oxide − O + N CHCH 2 CH 2 C Me 2 ( 4 ), at room temperature for 15 min, furnishes via [3+2] cycloaddition the fused bicyclic Δ 4 -1,2,4-oxadiazoline Pt(II) complexes trans- [PtCl 2 { N C(R)O N C(H)CH 2 CH 2 C Me 2 } 2 ] (R 1  = CH 2 CO 2 Me ( 5a ), R 2  = CH 2 Cl ( 5b )). Compounds 5a and 5b were refluxed in CH 2 Cl 2 for 1 week to afford the derived ketoimine Pt(II) complexes trans- [PtCl 2 {N(C( O)(R)) C CH 2 CH 2 C(Me 2 ) N H} 2 ] (R 1  = CH 2 CO 2 Me ( 6a ), R 2  = CH 2 Cl ( 6b )), respectively, as a result of the N–O bond cleavage of the oxadiazoline ring in 5 . The c…

Exergonic reactionBicyclic moleculeStereochemistryRegioselectivityPyrrolineCarbon-13 NMRMedicinal chemistryCycloadditionInorganic Chemistrychemistry.chemical_compoundchemistryMaterials ChemistryMoleculePhysical and Theoretical ChemistryBond cleavagePolyhedron
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Enhanced [4+2] cycloadditions by solvophobic effects and gravity-induced mixing in core-shell droplets

2017

A new way to perform reactions in core—shell double emulsions is reported herein. The phase boundaries of the threephase droplet flow were used to pressurize the reactants in the shell liquid, enhancing the reaction rate of a cycloaddition greatly in comparison to known methods. As key parameters, solvophobic effects and precise control over the droplet sizes were used to exploit a reaction with a negative volume of activation. The internal pressure of the reaction solution was regulated purely by the thickness of the shell liquid without adding additional reagents. Additionally, the reaction performed better when the core droplet was used to stir the shell droplet, considerably improving t…

Fluid Flow and Transfer Processes010405 organic chemistryChemistryOrganic ChemistryMixing (process engineering)Shell (structure)double emulsions010402 general chemistrymicroreactor01 natural sciences0104 chemical sciencesPhysics::Fluid DynamicsReaction rateChemistry (miscellaneous)Chemical physicsPhase (matter)Mass transferReagentPhysics::Atomic and Molecular Clustersactive mixingOrganic chemistryMicroreactorSolvophobichydrophobic effectcycloaddition
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Dual Enzyme-Responsive Capsules of Hyaluronic Acid-block-Poly(Lactic Acid) for Sensing Bacterial Enzymes.

2015

The synthesis of novel amphiphilic hyaluronic acid (HYA) and poly(lactic acid) (PLA) block copolymers is reported as the key element of a strategy to detect the presence of pathogenic bacterial enzymes. In addition to the formation of defined HYA-block-PLA assemblies, the encapsulation of fluorescent reporter dyes and the selective enzymatic degradation of the capsules by hyaluronidase and proteinase K are studied. The synthesis of the dual enzyme-responsive HYA-b-PLA is carried out by copper-catalyzed Huisgen 1,3-dipolar cycloaddition. The resulting copolymers are assembled in water to form vesicular structures, which are characterized by scanning electron microscopy, transmission electron…

Fluorescence-lifetime imaging microscopyStaphylococcus aureusMaterials sciencePolymers and PlasticsCell SurvivalPolymersDrug CompoundingPolyestersMolecular Sequence DataPrimary Cell CultureHyaluronoglucosaminidaseBiosensing TechniquesFluorescence spectroscopyNanocapsuleschemistry.chemical_compoundDynamic light scatteringBacterial ProteinsNanocapsulesHyaluronidaseAmphiphileMaterials ChemistrymedicineHumansLactic AcidHyaluronic AcidMicellesFluorescent DyesCycloaddition ReactionRhodaminesOrganic Chemistrytechnology industry and agricultureEndothelial CellsDermisLactic acidchemistryBiochemistryCarbohydrate SequencePseudomonas aeruginosaBiophysicsLiberationEndopeptidase Kmedicine.drugMacromolecular rapid communications
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18F-Labeling Using Click Cycloadditions

2014

Due to expanding applications of positron emission tomography (PET) there is a demand for developing new techniques to introduce fluorine-18 (t1/2=109.8 min). Considering that most novel PET tracers are sensitive biomolecules and that direct introduction of fluorine-18 often needs harsh conditions, the insertion of18F in those molecules poses an exceeding challenge. Two major challenges during18F-labeling are a regioselective introduction and a fast and high yielding way under mild conditions. Furthermore, attention has to be paid to functionalities, which are usually present in complex structures of the target molecule. The Cu-catalyzed azide-alkyne cycloaddition (CuAAC) and several copper…

Fluorine RadioisotopesGeneral Immunology and MicrobiologyCycloaddition ReactionStaining and LabelingComputer sciencelcsh:Rlcsh:MedicineNanotechnologyGeneral MedicineReview ArticleHigh yieldingGeneral Biochemistry Genetics and Molecular BiologyCycloadditionCatalysis18f labelingClick chemistryAnimalsClick ChemistryPet tracerCopperBioMed Research International
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Synthesis and Evaluation of Novel Ring‐Strained Noncanonical Amino Acids for Residue‐Specific Bioorthogonal Reactions in Living Cells

2021

Abstract Bioorthogonal reactions are ideally suited to selectively modify proteins in complex environments, even in vivo. Kinetics and product stability of these reactions are crucial parameters to evaluate their usefulness for specific applications. Strain promoted inverse electron demand Diels–Alder cycloadditions (SPIEDAC) between tetrazines and strained alkenes or alkynes are particularly popular, as they allow ultrafast labeling inside cells. In combination with genetic code expansion (GCE)‐a method that allows to incorporate noncanonical amino acids (ncAAs) site‐specifically into proteins in vivo. These reactions enable residue‐specific fluorophore attachment to proteins in living mam…

FluorophoreKinetics010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundIn vivoChemical BiologyAnimalsAmino AcidsFluorescent Dyeschemistry.chemical_classificationCycloaddition ReactionFull Paper010405 organic chemistryChemistryOrganic ChemistryProteinsprotein engineeringGeneral ChemistryProtein engineeringFull PapersGenetic codelive-cell labeling0104 chemical sciencesAmino acidkineticsAlkynesclick chemistryBiophysicsClick chemistryBioorthogonal chemistryunnatural amino acidsChemistry – A European Journal
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Synthesis of β- and γ-carbolines via ruthenium and rhodium catalysed [2+2+2] cycloadditions of yne-ynamides with methylcyanoformate

2011

A flexible approach towards substituted β- and γ-carbolines based on transition metal catalysed [2+2+2] cycloaddition reactions between functionalised yne-ynamides and methylcyanoformate is described. The versatility of this new reaction sequence is demonstrated by its application in the total synthesis of the marine natural product eudistomin U.

Formateschemistry.chemical_elementRutheniumCatalysisRhodiumCatalysischemistry.chemical_compoundTransition metalReaction sequenceMaterials ChemistryOrganic chemistryRhodiumNatural productMetals and AlloysTotal synthesisGeneral ChemistryCombinatorial chemistryCycloadditionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsRutheniumchemistryCyclizationAlkynesCeramics and CompositesCarbolinesChemical Communications
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Preparation and reactivity of macrocyclic dienynes

2010

Abstract (1 E ,5 E )-Cyclopentadeca-1,5-dien-3-yne ( 1c ), which represents the first macrocyclic 1,5-dien-3-yne, can be obtained by thermal- or butyllithium-induced fragmentation of the corresponding 1,2,3-selenadiazole 8 . The ( E , E )-dienyne functionality causes a geometrical strain E g , which enhances the reactivity in addition ( 1c → 12 , 13 ) and cycloaddition ( 1c → 10 ) reactions and lowers the isomerization barrier to the unstrained ( E , Z )-configuration 1d ( E g  = 0). A slow process 1c → 1d occurs even at ambient temperatures within several weeks.

Fragmentation (mass spectrometry)Strain (chemistry)StereochemistryChemistryOrganic ChemistryDrug DiscoveryReactivity (chemistry)BiochemistryMedicinal chemistryIsomerizationCycloadditionTetrahedron Letters
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MRI-Visible Poly(ε-caprolactone) with Controlled Contrast Agent Ratios for Enhanced Visualization in Temporary Imaging Applications

2013

International audience; Hydrophobic macromolecular contrast agents (MMCAs) are highly desirable to provide safe and efficient magnetic resonance (MR) visibility to implantable medical devices. In this study, we report on the synthesis and evaluation of novel biodegradable poly(ε-caprolactone)-based MMCAs. Poly(α-propargyl-ε-caprolactone-co-ε-caprolactone)s containing 2, 5, and 10 mol % of propargyl groups have been prepared by ring-opening copolymerization of ε-caprolactone and the corresponding propargylated lactone. In parallel, a diazido derivative of the clinically used diethylenetriaminepentaacetic acid (DTPA)/Gd3+ complex has been synthesized. Finally, MRI-visible poly(ε-caprolactone)…

Gadolinium DTPAPolymers and PlasticsMacromolecular SubstancesPolyestersContrast MediaBiocompatible MaterialsBioengineering02 engineering and technology010402 general chemistrybiomedical01 natural sciencesImagingBiomaterialsMicechemistry.chemical_compoundPoly(ε-caprolactone)Polymer chemistryMaterials ChemistryCopolymerAnimalsmacromolecularCell Proliferationchemistry.chemical_classificationMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistryMRI; Poly(ε-caprolactone); ImagingSpin–lattice relaxationFibroblastsHydrophobic[CHIM.ORGA] Chemical Sciences/Organic chemistry021001 nanoscience & nanotechnologyGraftingMagnetic Resonance ImagingvisibleCycloaddition0104 chemical sciencescopolymerizationchemistryPropargylDTPA0210 nano-technologyCaprolactoneLactoneMacromoleculeMRI
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Unveiling the Chemistry of Higher-Order Cycloaddition Reactions within the Molecular Electron Density Theory

2022

The higher-order cycloaddition (HOCA) reaction of tropone with cyclopentadiene (Cp) has been studied within the Molecular Electron Density Theory. The Electron Localization Function (ELF) analysis of the electronic structure of tropone and Cp characterizes the structural behaviors of the two conjugated unsaturated systems, while the conceptual DFT reactivity indices classify tropone as a strong electrophile and Cp as a strong nucleophile participating in polar cycloaddition reactions of reverse electron density flux. Eight competitive reaction paths have been characterized for this cycloaddition reaction. The most favorable one allowing the formation of the formal out [6 + 4] cycloadduct ha…

General Medicinehigher-order cycloaddition reactions; molecular electron density theory; molecular mechanism; tropone; selectivityChemistry; Volume 4; Issue 3; Pages: 735-752
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Sweet (hetero)aromatics: glycosylated templates for the construction of saccharide mimetics

2011

Mono- and diglycosylated aromatics and heteroaromatics may serve as building blocks for the construction of metabolically stable mimetics of oligosaccharides. Methods for their preparation from monosaccharidic precursors by direct C-glycosylation, dipolar cycloaddition or Larock cyclization are described.

GlycosylationChemistryMetals and AlloysOligosaccharidesmacromolecular substancesGeneral ChemistryHydrocarbons AromaticCombinatorial chemistryCatalysisCycloadditionSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsTemplateCyclizationMaterials ChemistryCeramics and CompositesOrganic chemistrylipids (amino acids peptides and proteins)Chemical Communications
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