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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:

The potential of click reactions for the synthesis of bioactive triterpenes
René Csük, Hans‐Peter Deigner
Bioorganic & Medicinal Chemistry Letters (2019) Vol. 29, Iss. 8, pp. 949-958
Closed Access | Times Cited: 45

Showing 1-25 of 45 citing articles:

Recent advances in 1,2,3- and 1,2,4-triazole hybrids as antimicrobials and their SAR: A critical review
Guimiao Tian, Qiuyi Song, Ziwei Liu, et al.
European Journal of Medicinal Chemistry (2023) Vol. 259, pp. 115603-115603
Closed Access | Times Cited: 49
Design and synthesis of pentacyclic triterpene conjugates and their use in medicinal research
Jiří Hodoň, Lucie Borková, J. Pokorný, et al.
European Journal of Medicinal Chemistry (2019) Vol. 182, pp. 111653-111653
Closed Access | Times Cited: 89
Structural modification strategies of triazoles in anticancer drug development
Qianwen Guan, Ziming Gao, Yuting Chen, et al.
European Journal of Medicinal Chemistry (2024) Vol. 275, pp. 116578-116578
Closed Access | Times Cited: 13
Asiatic acid as a leading structure for derivatives combining sub-nanomolar cytotoxicity, high selectivity, and the ability to overcome drug resistance in human preclinical tumor models
Oliver Kraft, Anne-Kathrin Hartmann, Sarah Brandt, et al.
European Journal of Medicinal Chemistry (2023) Vol. 250, pp. 115189-115189
Closed Access | Times Cited: 15
Synthesis of novel ursolic acid-gallate hybrids via 1,2,3-triazole linkage and its anti-oxidant and anti-inflammatory activity study
Zhiwen Qi, Pujun Xie, Zhihong Wang, et al.
Arabian Journal of Chemistry (2024) Vol. 17, Iss. 5, pp. 105762-105762
Open Access | Times Cited: 5
Potential Pharmacological Properties of Triterpene Derivatives of Ursolic Acid
Vuyolwethu Khwaza, Blessing A. Aderibigbe
Molecules (2024) Vol. 29, Iss. 16, pp. 3884-3884
Open Access | Times Cited: 5
Synthesis and Biological Activity of Derivatives of (C-30)-Substituted Lupane Triterpenoids and Gallic Acid Bound Through a 1,2,3-Triazole Linker
Sergey A. Popov, Zhiwen Qi, Guidong Yang, et al.
Chemistry of Natural Compounds (2025)
Closed Access
Click reactions: Recent trends in preparation of new sorbents and stationary phases for extraction and chromatographic applications
Sima Najafi Ghamat, Zahra Talebpour, Ahmad Mehdi
TrAC Trends in Analytical Chemistry (2019) Vol. 118, pp. 556-573
Closed Access | Times Cited: 33
Synthesis and cholinesterase inhibiting potential of A-ring azepano- and 3-amino-3,4-seco-triterpenoids
О. Б. Казакова, И. Е. Смирнова, T. V. Lopatina, et al.
Bioorganic Chemistry (2020) Vol. 101, pp. 104001-104001
Closed Access | Times Cited: 22
Synthesis and cytotoxicity of hybrids of 1,3,4- or 1,2,5-oxadiazoles tethered from ursane and lupane core with 1,2,3-triazole
Sergey A. Popov, Marya D. Semenova, Dmitry S. Baev, et al.
Steroids (2020) Vol. 162, pp. 108698-108698
Open Access | Times Cited: 22
Mechanisms, Copper Catalysts, and Ligands Involved in the Synthesis of 1,2,3- Triazoles Using Click Chemistry
Elisa Leyva, Irving Rubén Rodríguez-Gutiérrez, Edgar Moctezuma, et al.
Current Organic Chemistry (2023) Vol. 26, Iss. 23, pp. 2098-2121
Closed Access | Times Cited: 7
Design, synthesis and biological activity of 1,4-quinone moiety attached to betulin derivatives as potent DT-diaphorase substrate
Monika Kadela-Tomanek, Maria Jastrzębska, Krzysztof Marciniec, et al.
Bioorganic Chemistry (2020) Vol. 106, pp. 104478-104478
Closed Access | Times Cited: 20
Novel A-Ring Chalcone Derivatives of Oleanolic and Ursolic Amides with Anti-Proliferative Effect Mediated through ROS-Triggered Apoptosis
E. F. Khusnutdinova, Anastasiya V. Petrova, Zulfia R. Zileeva, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 18, pp. 9796-9796
Open Access | Times Cited: 16
Ester and amide derivatives of rhodamine B exert cytotoxic effects on different human tumor cell lines
Immo Serbian, Sophie Hoenke, Oliver Kraft, et al.
Medicinal Chemistry Research (2020) Vol. 29, Iss. 9, pp. 1655-1661
Open Access | Times Cited: 16
The presence of a cationic center is not alone decisive for the cytotoxicity of triterpene carboxylic acid amides
Benjamin Brandes, Lukas Koch, Sophie Hoenke, et al.
Steroids (2020) Vol. 163, pp. 108713-108713
Closed Access | Times Cited: 13
Cytotoxic Potential of a-Azepano- and 3-Amino-3,4-SeCo-Triterpenoids
О. Б. Казакова, И. Е. Смирнова, E. V. Tret’yakova, et al.
International Journal of Molecular Sciences (2021) Vol. 22, Iss. 4, pp. 1714-1714
Open Access | Times Cited: 12
An improved partial synthesis of corosolic acid and its conversion to highly cytotoxic mitocans
Niels V. Heise, Sophie Hoenke, Immo Serbian, et al.
European Journal of Medicinal Chemistry Reports (2022) Vol. 6, pp. 100073-100073
Open Access | Times Cited: 8
Diastereoselective Synthesis of Triterpenoid 1,2,4-Trioxolanes by Griesbaum Co-ozonolysis
О. Б. Казакова, E. F. Khusnutdinova, Anastasiya V. Petrova, et al.
Journal of Natural Products (2019) Vol. 82, Iss. 9, pp. 2550-2558
Closed Access | Times Cited: 13
Synthesis of C17-[5-methyl-1,3]-oxazoles by N-propargylation of triterpenic acids and evaluation of their cytotoxic activity
E. F. Khusnutdinova, Anastasiya V. Petrova, А. Н. Лобов, et al.
Natural Product Research (2020) Vol. 35, Iss. 21, pp. 3850-3858
Closed Access | Times Cited: 12
Synthesis of triazole AD-1 derivatives and its mechanism of mediating DNA damage of ROS in lung cancer cells
Linlin Han, Hongyan Tan, Jungjoon Lee, et al.
Bioorganic Chemistry (2024) Vol. 148, pp. 107457-107457
Closed Access | Times Cited: 1
Antitumor Effects of Triterpenes in Hepatocellular Carcinoma
Antoni Sureda, Miquel Martorell, Xavier Capó, et al.
Current Medicinal Chemistry (2020) Vol. 28, Iss. 13, pp. 2465-2484
Closed Access | Times Cited: 9
Alkynyl‐ or Azido‐Functionalized 1,2,3‐Triazoles: Selective MonoCuAAC Promoted by Physical Factors
Maxim A. Topchiy, Alexandra A. Ageshina, Gleb A. Chesnokov, et al.
ChemistrySelect (2019) Vol. 4, Iss. 25, pp. 7470-7475
Closed Access | Times Cited: 8
Preparation and Characterization of Thermal and pH Dual Sensitive Hydrogel Based on 1,3‐Dipole Cycloaddition Reaction
Hongliang Wei, Zijun Liu, Hongzheng Zhu, et al.
Polymer Engineering and Science (2020) Vol. 60, Iss. 5, pp. 917-924
Closed Access | Times Cited: 7
A Study of Plant Coumarins. 18. Conjugates of Coumarins with Lupane Triterpenoids and 1,2,3-Triazoles: Synthesis and Anti-Inflammatory Activity
Алла В. Липеева, М. П. Долгих, Т. Г. Толстикова, et al.
Russian Journal of Bioorganic Chemistry (2020) Vol. 46, Iss. 2, pp. 125-132
Closed Access | Times Cited: 7
New 30-substituted derivatives of pentacyclic triterpenes: preparation, biological activity, and molecular docking study
Elwira Chrobak, Ewa Bębenek, Krzysztof Marciniec, et al.
Journal of Molecular Structure (2020) Vol. 1226, pp. 129394-129394
Closed Access | Times Cited: 7
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