Bicyclic 6–6 Systems: Two Heteroatoms 1:1

Stanforth, Stephen P.

doi:10.1016/b978-008096518-5.00159-3

Cited by 8 publications

(2 citation statements)

References 133 publications

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“…The naphthyridines (NAPs) are a group of diazanaphthalenes that contain a single nitrogen atom in each ring but no nitrogen atom at either of the bridgehead positions [1]. Several structural isomers exist, where the 1,8-NAPs are key components of a number of antibacterial agents [2]. The synthetic procedure are prepared via the Friedländer condensation of 2-aminonicotinaldehyde with the corresponding acyl derivatives [3][4][5][6].…”

Section: Introductionmentioning

confidence: 99%

Catalytic activity in transfer hydrogenation using ruthenium (II) carbonyl complexes containing two 1,8-naphthyridine as N-monodentate ligands

Gajardo

Araya

Ibáñez

et al. 2019

Inorganica Chimica Acta

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, who retired recently. Professor Le Bozec had a long and fruitful collaboration with our group in Chile for 30 years. During that time many Chilean postgraduate students made part of their theses in the University of Rennes, supervised by Prof. Le Bozec. Throughout his collaboration with us, we have not only an excellent co-worker but also a great friend and we are sure that our friendship will last forever.

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Section: Introductionmentioning

confidence: 99%

Catalytic activity in transfer hydrogenation using ruthenium (II) carbonyl complexes containing two 1,8-naphthyridine as N-monodentate ligands

Gajardo

Araya

Ibáñez

et al. 2019

Inorganica Chimica Acta

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“…1,8-Naphthyridin-4-ones are a group of heterocycles that demonstrate biological activity toward numerous important targets. As a result there are many recent examples of preparing these compounds …”

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confidence: 99%

A Convenient One-Pot Synthesis of 1,8-Naphthyridones

et al. 2003

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In this paper, we disclose an efficient one-pot procedure for the preparation of substituted 1,8-naphthyridin-4-one analogues. Previous efforts to effect this type of transformation were complicated by the formation of benzene tricarboxylate. Via the use of excess base, the impurity formation was completely inhibited. This allowed for the clean preparation of the desired intermediate and subsequent formation of naphthyridone analogues in a single flask, which could then be crystallized directly from the reaction mixture in good yield and high purity.

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2007

Chemistry of Heterocyclic Compounds: A Series of Monographs

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Bicyclic 6–6 Systems: Two Heteroatoms 1:1

Cited by 8 publications

References 133 publications

Catalytic activity in transfer hydrogenation using ruthenium (II) carbonyl complexes containing two 1,8-naphthyridine as N-monodentate ligands

Catalytic activity in transfer hydrogenation using ruthenium (II) carbonyl complexes containing two 1,8-naphthyridine as N-monodentate ligands

A Convenient One-Pot Synthesis of 1,8-Naphthyridones

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