Search results for "cycloaddition reaction"

showing 10 items of 45 documents

A Molecular Electron Density Theory Study of the [3+2] Cycloaddition Reaction of Pseudo(mono)radical Azomethine Ylides with Phenyl Vinyl Sulphone

2022

The [3+2] cycloaddition (32CA) reaction of an azomethine ylide (AY), derived from isatin and L-proline, with phenyl vinyl sulphone has been studied within Molecular Electron Density Theory (MEDT) at the ωB97X-D/6-311G(d,p) level. ELF topological analysis of AY classifies it as a pseudo(mono)radical species with two monosynaptic basins at the C1 carbon, integrating a total of 0.76 e. While vinyl sulphone has a strong electrophilic character, AY is a supernucleophile, suggesting a high polar character and low activation energy for the reaction. The nucleophilic Parr functions indicate that the pseudoradical C1 carbon is the most nucleophilic center. The 32CA reaction presents an activat…

Molecular Electron Density Theory; azomethine ylides; [3+2] cycloaddition reaction; molecular mechanism; selectivity; reactivityGeneral Medicine
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Heterocycles from α-aminonitriles.

2014

Owing to their various modes of reactivity, α-aminonitriles represent versatile building blocks for the construction of a wide range of nitrogen heterocycles. The present Concept article focuses on synthetic methodologies using their bifunctional nature which is the basis of their reactivity as α-amino carbanions and as iminium ions. Reactions exclusively taking place on either the amine or on the nitrile moiety will not be considered.

NitrileAlkylationCycloaddition ReactionNitrogenOrganic ChemistryIminiumStereoisomerismGeneral ChemistryCarbonCatalysischemistry.chemical_compoundchemistryHeterocyclic CompoundsNitrilesOrganic chemistryMoietyAmine gas treatingReactivity (chemistry)IminesBifunctionalCarbanionChemistry (Weinheim an der Bergstrasse, Germany)
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Studies on the structure of coumarin-modified dextran nanoparticles by fluorescence spectroscopy.

2012

The photophysical and photochemical characteristics of nano-scaled particles obtained via solvent displacement from coumarin-modified dextrans were studied by means of absorption- and fluorescence-spectroscopy. The environment-dependent fluorescence emission of the pendant 4-methyl-7-alkoxy coumarin groups was exploited as a probe to gain information about the inner structure of the polysaccharide based nanoparticles. Time-resolved fluorescence measurements showed that the particles had two domains of different polarity and it could be confirmed that the core of the nano-assemblies contained water. Moreover, preliminary experiments were carried out demonstrating the possibility to control t…

Polymers and PlasticsCycloaddition Reactionta221Organic ChemistryNanoparticleDextransPhotochemistryCoumarinFluorescenceFluorescence spectroscopySolventchemistry.chemical_compoundDextranUltraviolet visible spectroscopySpectrometry FluorescencechemistryCoumarinsMaterials ChemistryNanoparticlesheterocyclic compoundsAbsorption (chemistry)ta116Carbohydrate polymers
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HPMA-Based Nanoparticles for Fast, Bioorthogonal iEDDA Ligation

2019

Contains fulltext : 216143.pdf (Publisher’s version ) (Open Access) Fast and bioorthogonally reacting nanoparticles are attractive tools for biomedical applications such as tumor pretargeting. In this study, we designed an amphiphilic block copolymer system based on HPMA using different strategies to introduce the highly reactive click units 1,2,4,5-tetrazines (Tz) either at the chain end (Tz-CTA) or statistical into the hydrophobic block. This reactive group undergoes a rapid, bioorthogonal inverse electron-demand Diels-Alder reaction (iEDDA) with trans-cyclooctenes (TCO). Subsequently, this polymer platform was used for the preparation of different Tz-covered nanoparticles, such as micell…

Polymers and PlasticsNanoparticleBioengineeringFluorescence correlation spectroscopy02 engineering and technologyConjugated system010402 general chemistry01 natural sciencesMicelleArticleBiomaterialsAmphiphileMaterials ChemistryCopolymerBenzene DerivativesColloidsMicellesPretargetingAza CompoundsCycloaddition ReactionChemistryOther Research Radboud Institute for Health Sciences [Radboudumc 0]021001 nanoscience & nanotechnologyCombinatorial chemistry0104 chemical sciencesCross-Linking ReagentsMethacrylatesNanoparticlesClick ChemistryBioorthogonal chemistry0210 nano-technology
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The influence of substitution in the quinoxaline nucleus on 1,3-dipolar cycloaddition reactions

2013

The reaction mechanism of 1,3-dipolar cycloadditions of both symmetric and unsymmetric benzo-condensed diazines with a nitrilimine dipole, to give two different mono- and bis-cycloadducts, in tetrahydrofuran (THF) solution, was studied by DFT calculatio ns. The results obtained show that each 1,3-dipolar cycloaddition reaction always proceeds by a two steps mechanism, in which the first intermediate shows only one covalent bond between the beta carbon of the nitrilimine and the aromatic nitrogen of the diazine molecule. The structure and energy content of the two transition states of the two cycloaddition steps, in the case of the unsymmetric benzo-condensed diazine, nicely explains why the…

Settore CHIM/03 - Chimica Generale E InorganicaSettore CHIM/08 - Chimica FarmaceuticaDFT calculations 13-Dipolar cycloaddition reactions Quinoxalines Reaction mechanism
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Amphiphilic Polyphenylene Dendron Conjugates for Surface Remodeling of Adenovirus 5

2020

Abstract Amphiphilic surface groups play an important role in many biological processes. The synthesis of amphiphilic polyphenylene dendrimer branches (dendrons), providing alternating hydrophilic and lipophilic surface groups and one reactive ethynyl group at the core is reported. The amphiphilic surface groups serve as biorecognition units that bind to the surface of adenovirus 5 (Ad5), which is a common vector in gene therapy. The Ad5/dendron complexes showed high gene transduction efficiencies in coxsackie‐adenovirus receptor (CAR)‐negative cells. Moreover, the dendrons offer incorporation of new functions at the dendron core by in situ post‐modifications, even when bound to the Ad5 sur…

Surface (mathematics)DendrimersCell SurvivalPolymersSurface PropertiesvirusesProtein CoronaCHO CellsGene delivery010402 general chemistry01 natural sciencesCatalysisAdenoviridaeTransduction (genetics)CricetulusCricetinaeDendrimerAmphiphilegene technologyAnimalsvirusesResearch ArticlesamphiphilesCycloaddition Reaction010405 organic chemistryChemistryBlood ProteinsGeneral MedicineGeneral ChemistryDendrimers | Hot PaperCombinatorial chemistryproteins0104 chemical sciencesLiposomesHydrophobic and Hydrophilic InteractionsBlood streamResearch ArticleProtein BindingConjugateAngewandte Chemie International Edition
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Unravelling [3+2] Cycloaddition Reactions through the Molecular Electron Density Theory

2018

Después de la primera clasificación de las reacciones 32CA en reacciones de tipo zw y pr, establecidas en el año 2014, la estructura y reactividad de los TACs más importantes utilizados en las reacciones 32CA ha sido completamente caracterizado en base a la MEDT propuesta recientemente. Entre la gran cantidad de trabajo desarrollado a lo largo de la presente tesis doctoral, se han seleccionado y discutido ocho publicaciones representativas, que permitieron caracterizar dos nuevos tipos de reactividad y consolidar la reactividad original de tipo zw. Así, dependiendo de las cuatro estructuras electrónicas diferentes de los TACs, es decir, pseudodiradical, pseudoradical, carbenoide y zwitterió…

[3+2] Cycloaddition ReactionsMolecular Electron Density TheoryMolecular MechanismsTheoretical Organic ChemistryOrganic Reactivity
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Kondrat'eva ligation: Diels-Alder-based irreversible reaction for bioconjugation.

2014

International audience; Diversification of existing chemoselective ligations is required to efficiently access complex and well-defined biomolecular assemblies with unique and valuable properties. The development and bioconjugation applications of a novel Diels-Alder-based irreversible site-specific ligation are reported. The strategy is based on a Kondrat'eva cycloaddition between bioinert and readily functionalizable 5-alkoxyoxazoles and maleimides that readily react together under mild and easily tunable reaction conditions to afford a fully stable pyridine scaffold. The potential of this novel bioconjugation is demonstrated through the preparation of fluorescent conjugates of biomolecul…

[CHIM.THER]Chemical Sciences/Medicinal ChemistryLigandsCatalysis[CHIM.ANAL]Chemical Sciences/Analytical chemistryFluorescence Resonance Energy TransferOrganic chemistryNuclear Magnetic Resonance BiomolecularOxazoleschemistry.chemical_classificationBioconjugationCycloaddition ReactionMolecular Structure[CHIM.ORGA]Chemical Sciences/Organic chemistryChemistryBiomoleculeOrganic Chemistry[CHIM.CATA]Chemical Sciences/CatalysisFluorescenceUrokinase-Type Plasminogen ActivatorCycloaddition[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryEnzyme ActivationFörster resonance energy transferLigationPlasminogen activator[CHIM.CHEM]Chemical Sciences/CheminformaticsConjugateThe Journal of organic chemistry
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Modular Assembly of Multimodal Imaging Agents through an Inverse Electron Demand Diels–Alder Reaction

2019

International audience; The combination of two imaging probes on a same biomolecule gives access to targeted bimodal imaging agents that can provide more accurate diagnosis, complementary information, or that may be used in different applications, such as PET imaging and fluorescence imagingassisted surgery. In this study, we demonstrate that dichlorotetrazine, a small, commercially available compound, can be used as a modular platform to easily assemble various imaging probes. Doubly-labeled tetrazines can then be conjugated to a protein through a biorthogonal IEDDA reaction. A series of difunctionalized tetrazine compounds containing various chelating agents and fluorescent dyes was synth…

[SDV.IB.IMA]Life Sciences [q-bio]/Bioengineering/ImagingTetrazineBiomedical EngineeringContrast MediaPharmaceutical SciencebimodalBioengineeringNanotechnology02 engineering and technology[CHIM.THER]Chemical Sciences/Medicinal ChemistryMultimodal ImagingProof of Concept Study01 natural sciencesMiceAnimalsHumansInverse electron-demand Diels–Alder reactionFluorescent DyesPharmacologyMultimodal imagingchemistry.chemical_classificationCycloaddition Reaction010405 organic chemistryChemistrybusiness.industryBiomoleculeOrganic ChemistryModular design021001 nanoscience & nanotechnology0104 chemical sciencestrastuzumabProof of conceptSPECT-CTSite-specificfluorescence0210 nano-technologybusinessBiotechnology
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Unveiling the Different Reactivity of Bent and Linear Three-Atom-Components Participating in [3 + 2] Cycloaddition Reactions

2021

The reactivity of a series of pairs of bent and linear three-atom-component (B-TACs and L-TACs) participating in [3 + 2] cycloaddition (32CA) reactions towards ethylene and electrophilic dicyanoethylene (DCE) have been studied within the Molecular Electron Density Theory. While the pseudodiradical structure of B-TACs changes to that of pseudoradical or carbenoid L-TACs upon dehydrogenation, zwitterionic B-TACs remain unchanged. Conceptual Density Functional Theory (CDFT) indices characterize five of the nine TACs as strong nucleophiles participating in polar reactions towards electrophilic ethylenes. The activation energies of the 32CA reactions with electrophilic DCE range from 0.5 to 22.0…

analytical_chemistry[3 + 2] cycloaddition reactionsOrganic chemistrychemical and pharmacologic phenomena010402 general chemistry01 natural sciencesQD241-441stomatognathic systemNucleophileComputational chemistrySingle bondReactivity (chemistry)skin and connective tissue diseasesCarbenoid010405 organic chemistryChemistrymolecular electron density theoryRegioselectivity16. Peace & justiceCycloaddition0104 chemical sciencesreactivitystomatognathic diseasesbent and linear three-atom-componentsregioselectivityElectrophileDensity functional theoryOrganics
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