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dc.contributor.authorMasdeu Margalef, Carme
dc.contributor.authorFuertes Sánchez, María ORCID
dc.contributor.authorMartín Encinas, Endika
dc.contributor.authorSelas Lanseros, Asier
dc.contributor.authorRubiales Alcaine, María Gloria ORCID
dc.contributor.authorPalacios Gambra, Francisco Javier ORCID
dc.contributor.authorAlonso Pérez, Concepción Estibaliz ORCID
dc.date.accessioned2020-09-04T08:48:51Z
dc.date.available2020-09-04T08:48:51Z
dc.date.issued2020-07-31
dc.identifier.citationMolecules 25(15) : (2020) // Article ID 3508es_ES
dc.identifier.issn1420-3049,
dc.identifier.urihttp://hdl.handle.net/10810/45986
dc.description.abstractHeterocyclic nitrogen compounds, including fused 1,5-naphthyridines, have versatile applications in the fields of synthetic organic chemistry and play an important role in the field of medicinal chemistry, as many of them have a wide range of biological activities. In this review, a wide range of synthetic protocols for the construction of this scaffold are presented. For example, Friedländer, Skraup, Semmlere-Wolff, and hetero-Diels-Alder, among others, are well known classical synthetic protocols used for the construction of the main 1,5-naphthyridine scaffold. These syntheses are classified according to the nature of the cycle fused to the 1,5-naphthyridine ring: carbocycles, nitrogen heterocycles, oxygen heterocycles, and sulphur heterocycles. In addition, taking into account the aforementioned versatility of these heterocycles, their reactivity is presented as well as their use as a ligand for metal complexes formation. Finally, those fused 1,5-naphthyridines that present biological activity and optical applications, among others, are indicated.es_ES
dc.description.sponsorshipFinancial support from the Ministerio de Ciencia, Innovación y Universidades (MCIU), Agencia Estatal de Investigación (AEI), Fondo Europeo de Desarrollo Regional (FEDER; RTI2018-101818-B-I00, UE), and by Gobierno Vasco, Universidad del País Vasco (GV, IT 992-16; UPV) is gratefully acknowledged.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/
dc.subjectfused 1,5-naphthyridineses_ES
dc.subjectheterocycle synthesises_ES
dc.subjectbiological activityes_ES
dc.subjectmetal complexeses_ES
dc.titleFused 1,5-Naphthyridines: Synthetic Tools and Applicationses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2020-08-07T13:38:38Z
dc.rights.holder2020 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.relation.publisherversionhttps://www.mdpi.com/1420-3049/25/15/3508es_ES
dc.identifier.doi10.3390/molecules25153508
dc.departamentoesQuímica orgánica I
dc.departamentoeuKimika organikoa I


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2020 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 2020 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/).