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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:

The Symbiotic Relationship Between Drug Discovery and Organic Chemistry
Oleksandr O. Grygorenko, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, et al.
Chemistry - A European Journal (2019) Vol. 26, Iss. 6, pp. 1196-1237
Closed Access | Times Cited: 141

Showing 1-25 of 141 citing articles:

Generating Multibillion Chemical Space of Readily Accessible Screening Compounds
Oleksandr O. Grygorenko, Dmytro S. Radchenko, Igor Dziuba, et al.
iScience (2020) Vol. 23, Iss. 11, pp. 101681-101681
Open Access | Times Cited: 153
Chemical Evolution of Natural Product Structure
Michael Grigalunas, Susanne Brakmann, Herbert Waldmann
Journal of the American Chemical Society (2022) Vol. 144, Iss. 8, pp. 3314-3329
Open Access | Times Cited: 139
Lewis acid catalyzed [4+2] annulation of bicyclobutanes with dienol ethers for the synthesis of bicyclo[4.1.1]octanes
Stefano Nicolai, Jérôme Waser
Chemical Science (2024) Vol. 15, Iss. 28, pp. 10823-10829
Open Access | Times Cited: 22
Emerging Building Blocks for Medicinal Chemistry: Recent Synthetic Advances
Oleksandr O. Grygorenko, Dmitriy M. Volochnyuk, Bohdan V. Vashchenko
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 47, pp. 6478-6510
Closed Access | Times Cited: 94
Small rings in the bigger picture: ring expansion of three- and four-membered rings to access larger all-carbon cyclic systems
Bohdan Biletskyi, P Colonna, Kévin Masson, et al.
Chemical Society Reviews (2021) Vol. 50, Iss. 13, pp. 7513-7538
Open Access | Times Cited: 83
A Close-up Look at the Chemical Space of Commercially Available Building Blocks for Medicinal Chemistry
Yuliana Zabolotna, Dmitriy M. Volochnyuk, Sergey V. Ryabukhin, et al.
Journal of Chemical Information and Modeling (2021) Vol. 62, Iss. 9, pp. 2171-2185
Open Access | Times Cited: 56
Mechanochemical C−X/C−H Functionalization: An Alternative Strategic Access to Pharmaceuticals
Xinjie Yang, Chongyang Wu, Weike Su, et al.
European Journal of Organic Chemistry (2022) Vol. 2022, Iss. 8
Closed Access | Times Cited: 44
Enabling Broader Adoption of Biocatalysis in Organic Chemistry
Evan O. Romero, Anthony Saucedo, José R. Hernández-Meléndez, et al.
JACS Au (2023) Vol. 3, Iss. 8, pp. 2073-2085
Open Access | Times Cited: 24
Spirocyclic compounds as innovative tools in drug discovery for medicinal chemists
Marina T. Varela, Gleiston G. Dias, Luiz Fernando N. de Oliveira, et al.
European Journal of Medicinal Chemistry (2025) Vol. 287, pp. 117368-117368
Closed Access | Times Cited: 1
Fragment-based drug discovery: opportunities for organic synthesis
Jeffrey D. St. Denis, Richard J. Hall, Christopher W. Murray, et al.
RSC Medicinal Chemistry (2020) Vol. 12, Iss. 3, pp. 321-329
Open Access | Times Cited: 51
DNA-encoded chemistry technology yields expedient access to SARS-CoV-2 M pro inhibitors
Srinivas Chamakuri, Shuo Lu, Melek N. Ucisik, et al.
Proceedings of the National Academy of Sciences (2021) Vol. 118, Iss. 36
Open Access | Times Cited: 47
Modern machine learning for tackling inverse problems in chemistry: molecular design to realization
Bhuvanesh Sridharan, Manan Goel, U. Deva Priyakumar
Chemical Communications (2022) Vol. 58, Iss. 35, pp. 5316-5331
Closed Access | Times Cited: 32
An extensive survey on the use of supervised machine learning techniques in the past two decades for prediction of drug side effects
Pranab Das, Dilwar Hussain Mazumder
Artificial Intelligence Review (2023) Vol. 56, Iss. 9, pp. 9809-9836
Open Access | Times Cited: 16
Six‐Membered Aromatic Nitrogen Heterocyclic Anti‐Tumor Agents: Synthesis and Applications
Jiatong Li, Ao Gu, Xiao‐Mei Nong, et al.
The Chemical Record (2023) Vol. 23, Iss. 12
Closed Access | Times Cited: 16
A divergent intermediate strategy yields biologically diverse pseudo-natural products
Sukdev Bag, Jie Liu, Sohan Patil, et al.
Nature Chemistry (2024) Vol. 16, Iss. 6, pp. 945-958
Open Access | Times Cited: 7
Poly(ADP-Ribose) Polymerase (PARP) Inhibitors for Cancer Therapy: Advances, Challenges, and Future Directions
Denys Bondar, Yevgen Karpichev
Biomolecules (2024) Vol. 14, Iss. 10, pp. 1269-1269
Open Access | Times Cited: 7
Bacterial catabolism of indole-3-acetic acid
Tyler S. Laird, Neptali Flores, Johan H. J. Leveau
Applied Microbiology and Biotechnology (2020) Vol. 104, Iss. 22, pp. 9535-9550
Closed Access | Times Cited: 46
Positional Analogue Scanning: An Effective Strategy for Multiparameter Optimization in Drug Design
Lewis D. Pennington, Brian Aquila, Younggi Choi, et al.
Journal of Medicinal Chemistry (2020) Vol. 63, Iss. 17, pp. 8956-8976
Closed Access | Times Cited: 43
Merging Directed C–H Activations with High-Throughput Experimentation: Development of Iridium-Catalyzed C–H Aminations Applicable to Late-Stage Functionalization
Erik Weis, Maria C. Johansson, Pernilla Korsgren, et al.
JACS Au (2022) Vol. 2, Iss. 4, pp. 906-916
Open Access | Times Cited: 27
Enrichment and purification of trace substances from yew extracum by twin-column recycling chromatography with a step solvent gradient
Wei Xie, Yuxue Wu, Guangxia Jin, et al.
Journal of Chromatography B (2025) Vol. 1252, pp. 124467-124467
Closed Access
Photoinduced synthesis of functionalized spiro[2.3]hexane via an additive-free approach
Dan Qi, Jinrui Bai, Yue Yao, et al.
Organic & Biomolecular Chemistry (2025)
Closed Access
Synthesis and Elaboration of Medium-Sized Ring Building Blocks Prepared via Cascade Ring Expansion Reactions
Haimei Zhou, Peter O’Brien, William P. Unsworth
The Journal of Organic Chemistry (2025)
Open Access
Photochemical [2 + 2] Cycloaddition of Alkenyl Boronic Derivatives: An Entry into 3-Azabicyclo[3.2.0]heptane Scaffold
Oleksandr P. Demchuk, Oleksandr V. Hryshchuk, Bohdan V. Vashchenko, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 9, pp. 5927-5940
Closed Access | Times Cited: 32
C–H functionalisation tolerant to polar groups could transform fragment-based drug discovery (FBDD)
Gianni Chessari, Rachel Grainger, Rhian S. Holvey, et al.
Chemical Science (2021) Vol. 12, Iss. 36, pp. 11976-11985
Open Access | Times Cited: 31
Advances in the synthesis of three-dimensional molecular architectures by dearomatizing photocycloadditions
Martins S. Oderinde, Soomin Jin, T. G. Murali Dhar, et al.
Tetrahedron (2021) Vol. 103, pp. 132087-132087
Closed Access | Times Cited: 27
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