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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:

Pyrrole: An insight into recent pharmacological advances with structure activity relationship
Shujauddin Ahmad, Ozair Alam, Mohd. Javed Naim, et al.
European Journal of Medicinal Chemistry (2018) Vol. 157, pp. 527-561
Closed Access | Times Cited: 198

Showing 1-25 of 198 citing articles:

1,2,3-Triazole-containing hybrids as leads in medicinal chemistry: A recent overview
Khurshed Bozorov, Jiangyu Zhao, Haji Akber Aisa
Bioorganic & Medicinal Chemistry (2019) Vol. 27, Iss. 16, pp. 3511-3531
Open Access | Times Cited: 659
Indole: A privileged scaffold for the design of anti-cancer agents
Yichao Wan, Yuanhua Li, Chunxing Yan, et al.
European Journal of Medicinal Chemistry (2019) Vol. 183, pp. 111691-111691
Closed Access | Times Cited: 379
Discovery of sulfadrug–pyrrole conjugates as carbonic anhydrase and acetylcholinesterase inhibitors
Mehmet Gümüş, Şemsi N. Babacan, Yeliz Demir, et al.
Archiv der Pharmazie (2021) Vol. 355, Iss. 1
Closed Access | Times Cited: 228
Synthesis of Biologically Active Molecules through Multicomponent Reactions
Daniel Insuasty, Juan‐Carlos Castillo, Diana Becerra, et al.
Molecules (2020) Vol. 25, Iss. 3, pp. 505-505
Open Access | Times Cited: 183
Synthetic heterocyclic candidates as promising α-glucosidase inhibitors: An overview
Manoj Dhameja, Preeti Gupta
European Journal of Medicinal Chemistry (2019) Vol. 176, pp. 343-377
Closed Access | Times Cited: 181
Sulfonamide derivatives as potential anti-cancer agents and their SARs elucidation
Yichao Wan, Guoqing Fang, Hongjuan Chen, et al.
European Journal of Medicinal Chemistry (2021) Vol. 226, pp. 113837-113837
Closed Access | Times Cited: 136
Therapeutic potential of pyrrole and pyrrolidine analogs: an update
N. Jeelan Basha, S. M. Basavarajaiah, K. Shyamsunder
Molecular Diversity (2022) Vol. 26, Iss. 5, pp. 2915-2937
Open Access | Times Cited: 114
Synthetic α-glucosidase inhibitors as promising anti-diabetic agents: Recent developments and future challenges
Alia Mushtaq, Uzma Azam, Saba Mehreen, et al.
European Journal of Medicinal Chemistry (2023) Vol. 249, pp. 115119-115119
Closed Access | Times Cited: 107
Target-based anticancer indole derivatives and insight into structure‒activity relationship: A mechanistic review update (2018–2021)
A M Dhiman, Rupam Sharma, Rajesh K. Singh
Acta Pharmaceutica Sinica B (2022) Vol. 12, Iss. 7, pp. 3006-3027
Open Access | Times Cited: 106
Versatile Synthetic Platform for 1,2,3-Triazole Chemistry
Disha P. Vala, Ruturajsinh M. Vala, Hitendra M. Patel
ACS Omega (2022) Vol. 7, Iss. 42, pp. 36945-36987
Open Access | Times Cited: 70
1,3,4-Oxadiazole-containing hybrids as potential anticancer agents: Recent developments, mechanism of action and structure-activity relationships
Swarnagowri Nayak, Santosh L. Gaonkar, Ebraheem Abdu Musad, et al.
Journal of Saudi Chemical Society (2021) Vol. 25, Iss. 8, pp. 101284-101284
Open Access | Times Cited: 73
Pd-Catalyzed Triple-Fold C(sp2)–H Activation with Enaminones and Alkenes for Pyrrole Synthesis via Hydrogen Evolution
Leiqing Fu, Yunyun Liu, Jie‐Ping Wan
Organic Letters (2021) Vol. 23, Iss. 11, pp. 4363-4367
Closed Access | Times Cited: 66
Novel 1, 2, 4-Triazoles as Antifungal Agents
Zahra Kazeminejad, Mahrokh Marzi, Abolfazl Alipour, et al.
BioMed Research International (2022) Vol. 2022, pp. 1-39
Open Access | Times Cited: 61
Pyrrole as an Important Scaffold of Anticancer Drugs: Recent Advances
Emilio Mateev, Maya Georgieva, Alexander Zlatkov
Journal of Pharmacy & Pharmaceutical Sciences (2022) Vol. 25, pp. 24-40
Open Access | Times Cited: 58
A Recent Overview of 1,2,3-Triazole-Containing Hybrids as Novel Antifungal Agents: Focusing on Synthesis, Mechanism of Action, and Structure-Activity Relationship (SAR)
Mahrokh Marzi, Mojtaba Farjam, Zahra Kazeminejad, et al.
Journal of Chemistry (2022) Vol. 2022, pp. 1-50
Open Access | Times Cited: 46
Copper-catalyzed C–H/N–H annulation of enaminones and alkynyl esters for densely substituted pyrrole synthesis
Leiqing Fu, Jie‐Ping Wan, Liyun Zhou, et al.
Chemical Communications (2022) Vol. 58, Iss. 11, pp. 1808-1811
Closed Access | Times Cited: 42
Molecular Editing of Pyrroles via a Skeletal Recasting Strategy
Xueting Zhou, Qingqin Huang, Jiami Guo, et al.
ACS Central Science (2023) Vol. 9, Iss. 9, pp. 1758-1767
Open Access | Times Cited: 21
Photocatalytic furan-to-pyrrole conversion
D.B. Kim, Jaehyun You, D. H. Lee, et al.
Science (2024) Vol. 386, Iss. 6717, pp. 99-105
Closed Access | Times Cited: 10
Pyrroles as Privileged Scaffolds in the Search for New Potential HIV Inhibitors
Maria da Conceição Avelino Dias Bianco, Débora Inácio Leite, Lucas Villas Bôas Hoelz, et al.
Pharmaceuticals (2021) Vol. 14, Iss. 9, pp. 893-893
Open Access | Times Cited: 49
A comprehensive survey upon diverse and prolific applications of chitosan-based catalytic systems in one-pot multi-component synthesis of heterocyclic rings
Hossein Mousavi
International Journal of Biological Macromolecules (2021) Vol. 186, pp. 1003-1166
Closed Access | Times Cited: 48
Flow synthesis approaches to privileged scaffolds – recent routes reviewed for green and sustainable aspects
Antonella Ilenia Alfano, Margherita Brindisi, Heiko Lange
Green Chemistry (2021) Vol. 23, Iss. 6, pp. 2233-2292
Closed Access | Times Cited: 45
Modular Domino Process toward Highly Functionalized Pyrroles via Pd-Catalyzed [4 + 1] Annulation under Mild Conditions
Linhong Zuo, Yulian Yang, Wusheng Guo
Organic Letters (2021) Vol. 23, Iss. 6, pp. 2013-2018
Closed Access | Times Cited: 42
Isocyanide-Based Multicomponent Reactions in Water: Advanced Green Tools for the Synthesis of Heterocyclic Compounds
Tahereh Nasiriani, Siamak Javanbakht, Mohammad Taghi Nazeri, et al.
Topics in Current Chemistry (2022) Vol. 380, Iss. 6
Closed Access | Times Cited: 31
Barton–Zard Reaction of β-Fluoro-β-nitrostyrenes─a Selective Route to Functionalized 4-Fluoropyrroles
Roman V. Larkovich, Victoria E. Shambalova, Savva A. Ponomarev, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 14, pp. 10122-10136
Closed Access | Times Cited: 17
Design, synthesis, in vitro anticancer, molecular docking and SAR studies of new series of pyrrolo[2,3-d]pyrimidine derivatives
Farid M. Sroor, Wael M. Tohamy, Khairy M. A. Zoheir, et al.
BMC Chemistry (2023) Vol. 17, Iss. 1
Open Access | Times Cited: 17
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