Fused 1,5-Naphthyridines: Synthetic Tools and Applications
dc.contributor.author | Masdeu Margalef, Carme | |
dc.contributor.author | Fuertes Sánchez, María | |
dc.contributor.author | Martín Encinas, Endika | |
dc.contributor.author | Selas Lanseros, Asier | |
dc.contributor.author | Rubiales Alcaine, María Gloria | |
dc.contributor.author | Palacios Gambra, Francisco Javier | |
dc.contributor.author | Alonso Pérez, Concepción Estibaliz | |
dc.date.accessioned | 2020-09-04T08:48:51Z | |
dc.date.available | 2020-09-04T08:48:51Z | |
dc.date.issued | 2020-07-31 | |
dc.identifier.citation | Molecules 25(15) : (2020) // Article ID 3508 | es_ES |
dc.identifier.issn | 1420-3049, | |
dc.identifier.uri | http://hdl.handle.net/10810/45986 | |
dc.description.abstract | Heterocyclic 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.sponsorship | Financial 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.iso | eng | es_ES |
dc.publisher | MDPI | es_ES |
dc.rights | info:eu-repo/semantics/openAccess | es_ES |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/es/ | |
dc.subject | fused 1,5-naphthyridines | es_ES |
dc.subject | heterocycle synthesis | es_ES |
dc.subject | biological activity | es_ES |
dc.subject | metal complexes | es_ES |
dc.title | Fused 1,5-Naphthyridines: Synthetic Tools and Applications | es_ES |
dc.type | info:eu-repo/semantics/article | es_ES |
dc.date.updated | 2020-08-07T13:38:38Z | |
dc.rights.holder | 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/). | es_ES |
dc.relation.publisherversion | https://www.mdpi.com/1420-3049/25/15/3508 | es_ES |
dc.identifier.doi | 10.3390/molecules25153508 | |
dc.departamentoes | Química orgánica I | |
dc.departamentoeu | Kimika organikoa I |
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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/).