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Authordc.contributor.authorAlmodovar, Iriux 
Authordc.contributor.authorRamírez Rodríguez, Oney es_CL
Authordc.contributor.authorBarriga, Andrés es_CL
Authordc.contributor.authorCaroli Rezende, Marcos es_CL
Authordc.contributor.authorAraya Maturana, Ramiro es_CL
Admission datedc.date.accessioned2011-10-12T14:52:48Z
Available datedc.date.available2011-10-12T14:52:48Z
Publication datedc.date.issued2011
Cita de ítemdc.identifier.citationRapid Commun. Mass Spectrom. 2011, 25, 370–378es_CL
Identifierdc.identifier.otherDOI: 10.1002/rcm.4868
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/121605
Abstractdc.description.abstractThe 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, Meerweintype rearrangements and dehydrations through elimination or intramolecular nucleophilic substitution.es_CL
Patrocinadordc.description.sponsorshipWe are grateful to CONICYT PBCT-PDA23, MECESUP UCH-116 and FONDECYT 1071077 grants for supporting this work. O. Ramı´rez-Rodrı´guez is grateful for MECESUP and DAAD PhD scholarships.es_CL
Lenguagedc.language.isoenes_CL
Publisherdc.publisherWileyes_CL
Títulodc.titleElectrospray ionization mass spectrometric fragmentation of hydroquinone derivativeses_CL
Document typedc.typeArtículo de revista


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