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• W2180212393 abstract "A series of 4-substituted 3-hydroxyfurazans were subjected to electrospray ionization tandem mass spectrometry. At low collision energy, oxyisocyanate ([O=C=N-O](-), m/z 58) was formed as the predominant product ion from each deprotonated 3-hydroxyfurazan, indicating cleavage of the heterocyclic ring. The facile energetics of this characteristic fragmentation process was confirmed by density functional computations." @default.
• W2180212393 created "2016-06-24" @default.
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• W2180212393 date "2015-11-17" @default.
• W2180212393 modified "2023-10-05" @default.
• W2180212393 title "Heterocyclic ring cleavage upon collision-induced dissociation of deprotonated 3-hydroxy-1,2,5-oxadiazoles (3-hydroxyfurazans)" @default.
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• W2180212393 doi "https://doi.org/10.1002/jms.3724" @default.
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