Fragmentation of plumeran indole alkaloids from Aspidosperma spruceanum by electrospray ionization tandem mass spectrometry |
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Authors: | Gabriela P. Aguiar Kamila A. L. Wakabayashi Guilherme F. Luz Vilma B. Oliveira Leda Mathias Ivo J. C. Vieira Raimundo Braz‐Filho Antonio E. M. Crotti |
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Affiliation: | 1. Núcleo de Pesquisas em Ciências Exatas e Tecnológicas, Universidade de Franca, 14404‐600 Franca‐SP, Brazil;2. Laboratório de Ciências Químicas (LCQUI)‐CCT, Universidade Estadual do Norte Fluminense Darcy Ribeiro (UENF), 28013‐602 Campos dos Goytacazes‐RJ, Brazil;3. Pesquisador Visitante Emerito–FAPERJ/UENF/UFRRJ, 28013‐602 Campos dos Goytacazes‐RJ, Brazil |
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Abstract: | The fragmentation of six plumeran indole alkaloids (PIAs) previously isolated from Aspidosperma spruceanum has been investigated by electrospray ionization tandem mass spectrometry (ESI‐MS/MS) in the positive ion mode. The fragmentation pathways have been established on the basis of MS/MS experiments using fragment ions generated in‐source and deuterium‐labeled alkaloids as precursor ions and on the basis of accurate mass measurements. Our results demonstrated that the fragmentation routes observed for the protonated PIAs are essentially derived from a pericyclic reaction and from the opening of rings D and E, followed by 1,4‐hydrogen rearrangements. Product ions resulting from radical eliminations were also observed, contrary to the ‘even‐electron rule’. Our data reveals that some product ions from protonated PIAs provide crucial information for the characterization of the acyl substituent at N‐1, the methoxyl and hydroxyl groups at the aromatic moiety, and give evidence of an ether bridge between C‐18 and C‐21. The data reported here were used for the dereplication of these compounds in a stem bark methanolic extract of Aspidosperma spruceanum. Copyright © 2010 John Wiley & Sons, Ltd. |
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