4.6 Review

Fused 1,5-Naphthyridines: Synthetic Tools and Applications

Journal

MOLECULES
Volume 25, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/molecules25153508

Keywords

fused 1; 5-naphthyridines; heterocycle synthesis; biological activity; metal complexes

Funding

  1. Ministerio de Ciencia, Innovacion y Universidades (MCIU), Agencia Estatal de Investigacion (AEI), Fondo Europeo de Desarrollo Regional (FEDER) (UE) [RTI2018-101818-B-I00]
  2. Gobierno Vasco, Universidad del Pais Vasco (GV) (UPV) [IT 992-16]

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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, Friedlander, 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.

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