Convenient one-step synthesis of 5-carboxy-seminaphthofluoresceins

Publication: Research - peer-reviewJournal article – Annual report year: 2017

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The one-step synthesis and characterization of a series of regioisomerically pure 5-carboxy-seminaphthofluoresceins (5-carboxy-SNAFLs) is reported. The optical properties were determined in aqueous buffer at around biological pH, and highly pH sensitive, large Stokes-shift fluorophores with emission in the deep-red to near-infrared region were identified
Original languageEnglish
JournalTetrahedron Letters
Volume58
Issue number16
Pages (from-to)1611-1615
ISSN0040-4039
DOIs
StatePublished - 2017
CitationsWeb of Science® Times Cited: No match on DOI

    Keywords

  • 5-Carboxy-seminaphthofluoresceins, Near-infrared-emitter, One-step synthesis, Enhanced Stokes shifts
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