Publication | Closed Access
Discovery of Fluorogenic Diarylsydnone-Alkene Photoligation: Conversion of <i>ortho</i>-Dual-Twisted Diarylsydnones into Planar Pyrazolines
82
Citations
37
References
2018
Year
EngineeringMolecular BiologySynthetic PhotochemistryOrganic ChemistryClick ChemistryChemistryHeterocycle ChemistryChemical BiologyAryl-pairing CombinationsFluorogenic Diarylsydnone-alkene PhotoligationPlanar PyrazolinesPhotochemistryBiochemistryMechanistic PhotochemistryFluorescent Turn-on LigationSupramolecular PhotochemistrySmall LibraryPhotochromismBiomolecular EngineeringNatural SciencesMolecular Switch
A small library of diarylsydnones (DASyds) was constructed based on aryl-pairing combinations and subjected to click reaction toward alkenes under photoirradiation with high efficiency. We were able to demonstrate the utility of DASyds for highly fluorescent turn-on ligation targeting the trans-cyclooct-4-en-1-ol moieties on protein.
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