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dc.contributor.authorLópez García, Luis Ángel
dc.contributor.authorGonzález-Pelayo, Silvia
dc.contributor.authorLópez, Enol
dc.contributor.authorBorge, Javier
dc.contributor.authorDe los Santos, Noemí
dc.date.accessioned2024-01-25T10:40:28Z
dc.date.available2024-01-25T10:40:28Z
dc.date.issued2018
dc.identifier.issn1434-193X
dc.identifier.urihttp://hdl.handle.net/10366/154721
dc.description.abstractThe InCl3-catalyzed reaction of ferrocene with ortho-hydroxybenzyl alcohols is reported and represents a convenient route for the synthesis of ferrocenyl phenols. This carbon–carbon bond forming process is believed to proceed through an ortho-quinone methide intermediate that can be intercepted by ferrocene through a Friedel–Crafts-type process. Preliminary cytotoxic screening carried out on several cancer cell lines revealed that some of the compounds exhibit moderate cytotoxicity.es_ES
dc.language.isoenges_ES
dc.titleFerrocene-Decorated Phenol Derivatives by Trapping ortho-Quinone Methide Intermediates with Ferrocenees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.projectIDCTQ2013-41511-P CTQ2013-40591-P CTQ2015-63567-R GRUPIN14-013 GRUPIN14-006 CTQ2016-76840-R CTQ2016-75986-Pes_ES
dc.rights.accessRightsinfo:eu-repo/semantics/openAccesses_ES


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