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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:

Chemical and chemoenzymatic stereoselective synthesis of β-nucleosides and their analogues
Hui-Jing Wang, Yang-Yang Zhong, You‐Cai Xiao, et al.
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 6, pp. 1719-1741
Closed Access | Times Cited: 11

Showing 11 citing articles:

Direct Synthesis of α- and β-2′-Deoxynucleosides with Stereodirecting Phosphine Oxide via Remote Participation
Xintong Tang, Yueer Zhou, Yingjie Wang, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 12, pp. 8768-8779
Closed Access | Times Cited: 8
Boronic Acid-Catalyzed Regio- and Stereoselective N-Glycosylations of Purines and Other Azole Heterocycles: Access to Nucleoside Analogues
Shrey P. Desai, Giorgos Yatzoglou, Julia A. Turner, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 7, pp. 4973-4984
Closed Access | Times Cited: 7
Synthesis of Nucleosides and Deoxynucleosides via Gold(I)-Catalyzed N-Glycosylation of Glycosyl (Z)-Ynenoates
Rongkun Liu, Yan Chen, Jibin Zheng, et al.
Organic Letters (2022) Vol. 24, Iss. 51, pp. 9479-9484
Closed Access | Times Cited: 22
Additive-controlled asymmetric iodocyclization enables enantioselective access to both α- and β-nucleosides
Qi Wang, Jiayi Mu, Jie Zeng, et al.
Nature Communications (2023) Vol. 14, Iss. 1
Open Access | Times Cited: 8
Folate Pathway Inhibitors, An Underestimated and Underexplored Molecular Target for New Anti-tuberculosis Agents
Sandra V. Vassiliades, Lara Gimenez Borges, Jeanine Giarolla, et al.
Mini-Reviews in Medicinal Chemistry (2023) Vol. 23, Iss. 17, pp. 1711-1732
Closed Access | Times Cited: 5
Is it still worth renewing nucleoside anticancer drugs nowadays?
Zai‐Qun Liu
European Journal of Medicinal Chemistry (2023) Vol. 264, pp. 115987-115987
Closed Access | Times Cited: 5
Mild Approach to Nucleoside Analogues via Photoredox/Cu-Catalyzed Decarboxylative C–N Bond Formation. Total Synthesis of Oxetanocin A
Ruonan Wang, Hao Xu, Arpan Banerjee, et al.
Organic Letters (2023) Vol. 26, Iss. 14, pp. 2691-2696
Closed Access | Times Cited: 5
Research progress in natural N-glycosides and synthetic methodologies for the formation of N-glycosidic bonds
Yingting Xia, Qingxia Xu, Alastair N. Herron, et al.
Science of Traditional Chinese Medicine (2024) Vol. 2, Iss. 2, pp. 82-94
Open Access
Synthesis of Natural and Sugar-Modified Nucleosides Using the Iodine/Triethylsilane System as N-Glycosidation Promoter
Martina Cimafonte, Anna Esposito, Maria De Fenza, et al.
International Journal of Molecular Sciences (2024) Vol. 25, Iss. 16, pp. 9030-9030
Open Access
An enantioselective and modular platform for C4ʹ-modified nucleoside analogue synthesis enabled by intramolecular trans-acetalizations
Nuligonda Thirupathi, Gautam Kumar, Jason W. Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access
Protecting-group-free synthesis of clevudine (l-FMAU), a treatment of the hepatitis B virus
Thomas Tremblay, Jessica B. Alcée, Denis Giguère
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 45, pp. 8859-8863
Closed Access | Times Cited: 3
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