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dc.contributor.authorCarral Menoyo, Asier
dc.contributor.authorOrtiz de Elguea Flecha, Verónica
dc.contributor.authorMartínez Nunes, Mikel ORCID
dc.contributor.authorSotomayor Anduiza, María Nuria
dc.contributor.authorLete Expósito, María Esther
dc.date.accessioned2018-04-09T08:49:40Z
dc.date.available2018-04-09T08:49:40Z
dc.date.issued2017-09
dc.identifier.citationMarine Drugs 15(9) : (2017) // Article ID 276es_ES
dc.identifier.issn1660-3397
dc.identifier.urihttp://hdl.handle.net/10810/26168
dc.description.abstractPalladium-catalyzed dehydrogenative coupling is an efficient synthetic strategy for the construction of quinoline scaffolds, a privileged structure and prevalent motif in many natural and biologically active products, in particular in marine alkaloids. Thus, quinolines and 1,2-dihydroquinolines can be selectively obtained in moderate-to-good yields via intramolecular C-H alkenylation reactions, by choosing the reaction conditions. This methodology provides a direct method for the construction of this type of quinoline through an efficient and atom economical procedure, and constitutes significant advance over the existing procedures that require preactivated reaction partners.es_ES
dc.description.sponsorshipMinisterio de Economia y Competitividad (CTQ2013-41229-P, CTQ2016-74881-P), Gobierno Vasco (IT1045-16) and Universidad del Pais Vasco/Euskal Herriko Unibertsitatea UPV/EHU are gratefully acknowledged for their financial support. V.O.-d.-E., A.C.-M. wish to thank Gobierno Vasco for grants. Technical and human support provided by Servicios Generales de Investigacion SGIker (UPV/EHU, MINECO, GV/EJ, ERDF and ESF) is also acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2013-41229-Pes_ES
dc.relationinfo:eu-repo/grantAgreement/MINECO/CTQ2016-74881-Pes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectquinolinees_ES
dc.subjectsynthesises_ES
dc.subjectpalladiumes_ES
dc.subjectcouplinges_ES
dc.subjectC-H alkenylationes_ES
dc.subjectmarine natural-productses_ES
dc.subjectC-H functionalizationes_ES
dc.subjectpyridoacridine alkalloidses_ES
dc.subjectbond functionalizationes_ES
dc.subjectindole-derivativeses_ES
dc.subjectalkenylationes_ES
dc.subjectheterocycleses_ES
dc.subjectolefinationes_ES
dc.subjectcyclizationes_ES
dc.subjectselectivityes_ES
dc.titlePalladium-Catalyzed Dehydrogenative Coupling: An Efficient Synthetic Strategy for the Construction of the Quinoline Corees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttp://www.mdpi.com/1660-3397/15/9/276es_ES
dc.identifier.doi10.3390/md15090276
dc.departamentoesQuímica orgánica IIes_ES
dc.departamentoeuKimika organikoa IIes_ES


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© 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access
article distributed under the terms and conditions of the Creative Commons Attribution
(CC BY) license (http://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's license is described as © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).