Abstract
A cyanide anion (CN-)-triggered deprotection of NH-protected phenothiazine, (E)-10-(10H-phenothiazin-3′-yl)propenal, has been discovered as a novel mechanism for the highly selective fluorescence detection of CN- under ambient conditions. The present protocol may pave the way for its broad application in organic synthesis in the near future. This journal is
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CITATION STYLE
APA
Garg, B., & Ling, Y. C. (2015). A highly selective phenothiazine-based fluorescence “turn-on” indicator based on cyanide-promoted novel protection/deprotection mechanism. Chemical Communications, 51(42), 8809–8812. https://doi.org/10.1039/c5cc01626f
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