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dc.contributor.authorMartínez-Montero, Lía-
dc.contributor.authorDíaz-Rodríguez, Alba-
dc.contributor.authorGotor, Vicente-
dc.contributor.authorGotor-Fernández, Vicente-
dc.contributor.authorLavandera, Iván-
dc.date.accessioned2016-06-01T06:07:18Z-
dc.date.available2016-06-01T06:07:18Z-
dc.date.issued2015-03-30-
dc.identifier.citationMartínez-Montero, L.; Díaz-Rodríguez, A.; Gotor, V.; Gotor-Fernández, V.; Lavandera, I. Broadening the Chemical Scope of Laccases: Selective Deprotection of N-Benzyl Groups. Green Chem., 2015, 17, 2794-2798.eng
dc.identifier.otherDOI: 10.1039/C5GC00525F-
dc.identifier.urihttps://ria.asturias.es/RIA/handle/123456789/6381-
dc.descriptionEl sistema catalítico formado por la lacasa de Trametes versicolor y el TEMPO es utilizado de forma eficiente para llevar a cabo la desprotección quimioselectiva de los grupos N-bencilo primarios en condiciones suaves de reacción.eng
dc.description.abstractLaccase from Trametes versicolor together with TEMPO has been found as a very efficient system to deprotect Nbenzylated primary amines, differing from previously described methods since it uses oxygen as mild oxidant in aqueous medium. Chemoselective removal of the benzyl group was achieved with excellent yields when secondary amine and alcohol moieties were also presenteng
dc.description.sponsorshipMICINN (Projects CTQ2011-24237 and CTQ2013-44153). Principado de Asturias (predoctoral fellowship Severo Ochoa).eng
dc.language.isoengeng
dc.publisherRoyal Society of Chemistry (RSC)eng
dc.relation.isreferencedbySí, esta versión ha sido citadaeng
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dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
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dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
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dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectQuímica Orgánicaeng
dc.subjectBiocatálisiseng
dc.subject.classificationPublicadoeng
dc.titleBroadening the Chemical Scope of Laccases: Selective Deprotection of N-Benzyl Groupseng
dc.typepostereng
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Química

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