0000000000358626

AUTHOR

Kévin Renault

showing 5 related works from this author

Rapid Synthesis of Unsymmetrical Sulforhodamines Through Nucleophilic Amination of a Monobrominated Sulfoxanthene Dye

2014

A transition-metal-free method for the synthesis of N-substituted unsymmetrical sulforhodamine fluorophores from an unusual monobrominated sulfoxanthene dye and primary or secondary amines by direct SNAr-type reactions is presented. The simplicity and effectiveness of this “postamination” procedure were demonstrated through the rapid preparation of a library of multifunctional red-emitting rhodamine analogues. Some of these analogues are equipped with a reactive handle and retain the two water-solubilizing sulfonic acid moieties of the starting halogenated derivative; this makes them ideal candidates for biolabeling applications. The potential utility of this expeditious strategy to finely …

chemistry.chemical_classification010405 organic chemistryOrganic ChemistrySulfonic acid010402 general chemistryPhotochemistry01 natural sciences7. Clean energyFluorescence0104 chemical sciencesRhodaminechemistry.chemical_compoundchemistryCyclenNucleophileNucleophilic substitutionAmine gas treatingPhysical and Theoretical ChemistryAminationEuropean Journal of Organic Chemistry
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Fluorogenic Enzyme-Triggered Domino Reactions Producing Quinoxalin-2(1H)-one-based Heterocycles

2020

International audience; A simple and effective biocompatible domino reaction triggered by a model protease and leading to formation of strongly fluorescent quinoxalin-2(1H)-one N-heterocycles is described. Some positive attributes including versatility and ability to provide outstanding fluorescence "OFF-ON" responses were revealed by this work. They open the way for practical applications of this novel type of "covalent-assembly" based fluorescent probes in the fields of sensing and bioimaging. Among the myriad of synthetic transformations and catalysts currently available for concise and efficient synthesis of organic molecules, bioinspired approaches based on the use of enzymes often int…

chemistry.chemical_classificationProtease[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistrymedicine.medical_treatmentOrganic Chemistry010402 general chemistryBiocompatible material01 natural sciencesBiochemistryCombinatorial chemistryFluorescenceDomino0104 chemical sciencesEnzymeCascade reactionmedicinePhysical and Theoretical ChemistryOrganic Letters
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A Novel Enzyme-Triggered Domino Reaction Producing Fluorescent Quinoxalin-2(1H)-One-Based Heterocycles

2020

A simple and effective biocompatible domino reaction triggered by a model protease and leading to formation of strongly fluorescent quinoxalin-2(1H)-one N-heterocycles is described. Some positive attributes including versatility and ability to provide outstanding fluorescence "OFF-ON" responses were revealed by this work. They open the way for practical applications of this novel type of "covalent-assembly" based fluorescent probes in the fields of sensing and bioimaging.; A simple and effective biocompatible domino reaction triggered by a model protease and leading to formation of strongly fluorescent quinoxalin-2(1H)-one N-heterocycles is described. Some positive attributes including vers…

In situchemistry.chemical_compoundFluorophorechemistryCascade reaction[CHIM.ORGA]Chemical Sciences/Organic chemistryLight emissionBioorthogonal chemistryBiosensorFluorescenceCombinatorial chemistryDomino
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Design, Synthesis and Evaluation of Enzyme-Responsive Fluorogenic Probes Based on Pyridine-Flanked Diketopyrrolopyrrole Dyes

2020

The ever-growing demand for fluorogenic dyes usable in the rapid construction of analyte-responsive fluorescent probes, has recently contributed to a revival of interest in the chemistry of diketopyrrolopyrrole (DPP) pigments. In this context, we have explored the potential of symmetrical and unsymmetrical DPP derivatives bearing two or one 4-pyridyl substituents acting as optically tunable group(s). The unique fluorogenic behavior of these molecules, closely linked to N-substitution/charge state of their pyridine unit (i.e., neutral pyridine or cationic pyridinium), has been used to design DPP-based fluorescent probes for detection of hypoxia-related redox enzymes and penicillin G acylase …

Aqueous solutionPyridinesCationic polymerizationContext (language use)02 engineering and technologyKetones010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescenceCombinatorial chemistryAtomic and Molecular Physics and Optics0104 chemical sciencesAnalytical Chemistrychemistry.chemical_compoundchemistryPyridineMoleculePyrrolesPyridinium0210 nano-technologyInstrumentationBiosensorSpectroscopyFluorescent Dyes
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Synthetic routes to novel fluorogenic pyronins and silicon analogs with far-red spectral properties and enhanced aqueous stability

2020

Fluorogenic detection of reactive (bio)analytes is often achieved with "smart" probes, whose activation mechanism causes the release of aniline-based fluorophores. Indeed, the protection-deprotection of their primary amino is the simplest way to induce dramatic and valuable changes in spectral features of the fluorogenic reporter. In this context, and due to their small size and intrinsic hydrophilicity, we focused on pyronin dyes and related heteroatom analogs (i.e., formal derivatives of 3-imino-3H-xanthen-6-amine and its silicon analog) for their use as optically tunable aniline-based fluorophores. To overcome some severe limitations associated with the use of such fluorogenic scaffolds …

Aqueous solutionSilicon[CHIM.ORGA]Chemical Sciences/Organic chemistryProcess Chemistry and TechnologyGeneral Chemical EngineeringHeteroatomchemistry.chemical_elementContext (language use)02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryFluorescence0104 chemical scienceschemistry.chemical_compoundAnilinechemistryElectrophile[CHIM]Chemical Sciences0210 nano-technologyJulolidine
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