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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Synthetic Strategies, Reactivity and Applications of 1,5-Naphthyridines
Marı́a Fuertes, Carme Masdeu, Endika Martín‐Encinas, et al.
Molecules (2020) Vol. 25, Iss. 14, pp. 3252-3252
Open Access | Times Cited: 9

Showing 9 citing articles:

New dinuclear gold(III) complex with 1,5-naphthyridine as bridging ligand: synthesis, characterization, DNA/BSA binding studies, and anticancer activity
Snežana Radisavljević, Dušan Ćoćić, Biljana Petrović, et al.
Gold bulletin (2024) Vol. 57, Iss. 1-2, pp. 9-25
Open Access | Times Cited: 2
Discovery of new naphthyridine hybrids against enoyl-ACP reductase (inhA) protein target of Mycobacterium tuberculosis: Molecular docking, molecular dynamics simulations studies
Govindaraj Sabarees, V. Velmurugan, V. Raja Solomon
Chemical Physics Impact (2023) Vol. 7, pp. 100399-100399
Open Access | Times Cited: 4
Speciation and kinetics of fluoride transfer from tetra-n-butylammonium difluorotriphenylsilicate (‘TBAT’)
Maciej M. Kucharski, Allan J. B. Watson, Guy C. Lloyd‐Jones
Chemical Science (2023) Vol. 15, Iss. 12, pp. 4331-4340
Open Access | Times Cited: 3
Mechanochemical Aza-Vinylogous Povarov Reactions for the Synthesis of Highly Functionalized 1,2,3,4-Tetrahydroquinolines and 1,2,3,4-Tetrahydro-1,5-Naphthyridines
José Clerigué, M. Teresa Ramos, J. Carlos Menéndez
Molecules (2021) Vol. 26, Iss. 5, pp. 1330-1330
Open Access | Times Cited: 7
New dinuclear gold(III) complex with 1,5-naphthyridine as bridging ligand: Synthesis, characterization, DNA/BSA binding studies and anticancer activity
Snežana Radisavljević, Dušan Ćoćić, Biljana Petrović, et al.
Research Square (Research Square) (2024)
Open Access
Synthesis of Dibenzo[b,h][1,5]naphthyridin-7(12H)-ones: The Pictet–Spengler Reaction versus a Rearrangement of 4-Phenyl[1,3]oxazolo[4,5-c]quinolines
Alexander S. Fisyuk, Антон Л. Шацаускас, Sergey A. Kirnosov, et al.
Synthesis (2024) Vol. 56, Iss. 13, pp. 2100-2108
Closed Access
The literature of heterocyclic chemistry, Part XX, 2020
Л. И. Беленький, Галина А. Газиева, Yu. B. Evdokimenkova, et al.
Advances in heterocyclic chemistry (2022), pp. 201-274
Closed Access | Times Cited: 2
Naphthyridine Derivatives Induce Programmed Cell Death in Naegleria fowleri
Aitor Rizo-Liendo, Iñigo Arberas-Jiménez, Endika Martín‐Encinas, et al.
Pharmaceuticals (2021) Vol. 14, Iss. 10, pp. 1013-1013
Open Access | Times Cited: 2
Development of methodologies for synthesis of 4-hydroxy-[1,5]naphthyridine-3-carbonitriles
Shashikala Kethireddy, D. Ramesh, Bhaskar Pittala, et al.
Materials Today Proceedings (2023) Vol. 92, pp. 498-500
Closed Access
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