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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:

An access to a library of novel triterpene derivatives with a promising pharmacological potential by Ugi and Passerini multicomponent reactions
Jana Wiemann, Lucie Heller, René Csük
European Journal of Medicinal Chemistry (2018) Vol. 150, pp. 176-194
Closed Access | Times Cited: 19

Showing 19 citing articles:

Multicomponent Reaction-Assisted Drug Discovery: A Time- and Cost-Effective Green Approach Speeding Up Identification and Optimization of Anticancer Drugs
Giovanni Graziano, Angela Stefanachi, Marialessandra Contino, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 7, pp. 6581-6581
Open Access | Times Cited: 44
Synthesis of N-2(5H)-furanonyl sulfonyl hydrazone derivatives and their biological evaluation in vitro and in vivo activity against MCF-7 breast cancer cells
Kai Yang, Jianqiong Yang, Shi‐He Luo, et al.
Bioorganic Chemistry (2020) Vol. 107, pp. 104518-104518
Closed Access | Times Cited: 46
Transformation of asiatic acid into a mitocanic, bimodal-acting rhodamine B conjugate of nanomolar cytotoxicity
Michael Kahnt, Jana Wiemann, Lucie Fischer, et al.
European Journal of Medicinal Chemistry (2018) Vol. 159, pp. 143-148
Closed Access | Times Cited: 38
Effective strategy for polymer synthesis: multicomponent reactions and click polymerization
Chang Wang, Bing Yu, Wenlong Li, et al.
Materials Today Chemistry (2022) Vol. 25, pp. 100948-100948
Closed Access | Times Cited: 22
Abietic, maleopimaric and quinopimaric dipeptide Ugi-4CR derivatives and their potency against influenza A and SARS-CoV-2
E. V. Tret’yakova, Xinyuan Ma, О. Б. Казакова, et al.
Natural Product Research (2022) Vol. 37, Iss. 12, pp. 1954-1960
Open Access | Times Cited: 11
Cytotoxic Dehydroabietylamine Derived Compounds
Jana Wiemann, Ahmed Al‐Harrasi, René Csük
Anti-Cancer Agents in Medicinal Chemistry (2020) Vol. 20, Iss. 15, pp. 1756-1767
Closed Access | Times Cited: 16
Synthesis of Novel Diterpenic Peptides via the Ugi Reaction and Their Anticancer Activities
Anna Smirnova, Liana Zakirova, И. Е. Смирнова, et al.
Molbank (2023) Vol. 2023, Iss. 3, pp. M1707-M1707
Open Access | Times Cited: 5
Bioactivities and Structure‐Activity Relationships of Maslinic Acid Derivatives: A Review
Rui Yan, Luguang Liu, Xing Huang, et al.
Chemistry & Biodiversity (2023) Vol. 21, Iss. 2
Closed Access | Times Cited: 5
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
Derivatization of Abietane Acids by Peptide-like Substituents Leads to Submicromolar Cytotoxicity at NCI-60 Panel
E. V. Tret’yakova, Anna Smirnova, Denis A. Babkov, et al.
Molecules (2024) Vol. 29, Iss. 15, pp. 3532-3532
Open Access | Times Cited: 1
Late‐stage functionalization of Vouacapane derivatives from Caesalpinia platyloba by a Groebke−Blackburn−Bienaymé reaction
Gabriela Servín‐García, Luis Chacón‐García, Alejandro Islas‐Jácome, et al.
Journal of Heterocyclic Chemistry (2023) Vol. 60, Iss. 11, pp. 1903-1910
Closed Access | Times Cited: 3
Dehydroabietylamine derived bistetrazoles from ultrasound-assisted pseudo-seven-component Ugi reactions act as efficient and selective inhibitors of cholinesterases
Niels V. Heise, Antonia Schmidt, Jördis‐Ann Schüler, et al.
European Journal of Medicinal Chemistry Reports (2023) Vol. 10, pp. 100124-100124
Open Access | Times Cited: 2
New Cytotoxic α‐Aminoacylamide and bis‐1,5‐Disubstituted Tetrazole Adducts From Amino‐Diterpene Molecules by Ugi Reaction
Anna Smirnova, E. V. Tret’yakova, О. Б. Казакова
Chemical Biology & Drug Design (2024) Vol. 104, Iss. 3
Closed Access
An Efficient and Facile Synthesis of tert‐Butyl 2‐(Methylamino)‐3‐nitro‐5‐oxo‐4‐aryl‐7,8‐dihydro‐4H‐pyrano[3,2‐c]pyridine‐6(5H)‐carboxylate derivatives in [BMIM]BF4
Zhengbing Pan, Hui Xu, Kaimin Mao, et al.
Journal of Heterocyclic Chemistry (2019) Vol. 56, Iss. 4, pp. 1393-1402
Closed Access | Times Cited: 2
Efficient Multicomponent Synthesis of Novel Rhodanine Based Amide Derivatives
Robabeh Baharfar, Mehrasa Tarahomi, Razieh Azimi
Organic Preparations and Procedures International (2019) Vol. 51, Iss. 6, pp. 595-601
Closed Access | Times Cited: 2
Synthesis of Bis-Amides Employing a Plant-Derived Triterpenoid as Component in the Ugi Reaction
Fidel Rodríguez-López, Hugo A. García‐Gutiérrez, Rocío Gámez‐Montaño
The 17th International Electronic Conference on Synthetic Organic Chemistry (2022), pp. 37-37
Open Access | Times Cited: 1
Plant-Derived Triterpenoid Functionalization: Synthesis of α-Acyloxycarboxamides
Fidel Rodríguez-López, Edgar G. Rodríguez-García, Hugo A. García‐Gutiérrez, et al.
(2023), pp. 102-102
Open Access
Catalyst-free synthesis of acenaphthoindolopyrimidine derivatives
Nahale Kakavand, Mohammad Bayat, Yadollah Bayat
Molecular Diversity (2022) Vol. 27, Iss. 4, pp. 1785-1793
Closed Access
Synthesis of Triterpenoid-Derived α-Acyloxycarboxamides via Passerini Reaction
Fidel Rodríguez-López, Hugo A. García‐Gutiérrez, Rocío Gámez‐Montaño
The 17th International Electronic Conference on Synthetic Organic Chemistry (2021), pp. 51-51
Open Access
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