Electrospray ionization mass spectrometric fragmentation of hydroquinone derivatives

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Electrospray ionization mass spectrometric fragmentation of hydroquinone derivatives.

The fragmentation patterns of nine di-, tri- and tetracyclic hydroquinones with potential antitumor activity were rationalized by invoking competing mechanisms that included sterically accelerated homolytic cleavage, Meerwein-type rearrangements and dehydrations through elimination or intramolecular nucleophilic substitution.

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ژورنال

عنوان ژورنال: Rapid Communications in Mass Spectrometry

سال: 2011

ISSN: 0951-4198

DOI: 10.1002/rcm.4929