Electron ionization mass spectrometric fragmentation and multiple reaction monitoring quantification of trimethylsilyl derivatives of cucurbic acid and its 6,7-stereoisomers - Archive ouverte HAL Accéder directement au contenu
Article Dans Une Revue Rapid Communications in Mass Spectrometry Année : 2016

Electron ionization mass spectrometric fragmentation and multiple reaction monitoring quantification of trimethylsilyl derivatives of cucurbic acid and its 6,7-stereoisomers

Marie Aimee Galeron
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Claude Aubert
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Résumé

Isomeric cucurbic acids derive from the reduction of the keto group of jasmonic acids. These growth regulators are natural constituents of various higher plants and fungi. Elucidation of electron ionization mass spectrometry (EIMS) fragmentation pathways of the trimethylsilyl (TMS) derivatives of the different stereoisomers is essential for their characterization and quantification in natural samples.

Dates et versions

hal-01438754 , version 1 (18-01-2017)

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Jean-Francois Rontani, Marie Aimee Galeron, Claude Aubert. Electron ionization mass spectrometric fragmentation and multiple reaction monitoring quantification of trimethylsilyl derivatives of cucurbic acid and its 6,7-stereoisomers. Rapid Communications in Mass Spectrometry, 2016, 30 (20), pp.2253-2264. ⟨10.1002/rcm.7711⟩. ⟨hal-01438754⟩
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