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dc.contributor.authorGodino Ojer, Marina
dc.contributor.authorShamzhy, Mariya
dc.contributor.authorČejka, Jiři
dc.contributor.authorPérez-Mayoral, Elena
dc.date.accessioned2020-01-30T11:02:08Z
dc.date.available2020-01-30T11:02:08Z
dc.date.issued2019
dc.identifier.issn0920-5861spa
dc.identifier.urihttp://hdl.handle.net/10641/1842
dc.description.abstractWe report here efficient synthesis of quinoxalines from ophenylendiamine and -hydroxy ketones over commercial Basolites. The concentration and type of acid centres, as CUS sites, together with the porosity of the samples strongly influence the resulting conversion and selectivity. Our results indicate a new reaction route in which tautomerization reactions are also involved.spa
dc.language.isoengspa
dc.publisherCatalysis Todayspa
dc.rightsAtribución-NoComercial-SinDerivadas 3.0 España*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es/*
dc.subjectBasolitesspa
dc.subjectMetal-Organic-Frameworksspa
dc.subjectNanocatalystsspa
dc.subjectFine chemicalsspa
dc.subjectQuinoxalinesspa
dc.titleBasolites: a type of Metal Organic Frameworks highly efficient in the one-pot synthesis of quinoxalines from a-hydroxy ketones under aerobic conditions.spa
dc.typearticlespa
dc.description.versionpre-printspa
dc.rights.accessRightsopenAccessspa
dc.description.extent624 KBspa
dc.identifier.doi10.1016/j.cattod.2019.08.002spa
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/abs/pii/S0920586119304237spa


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Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 España