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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:

Recent applications of isatin in the synthesis of organic compounds
Razieh Moradi, Ghodsi Mohammadi Ziarani, Negar Lashgari
ARKIVOC (2017) Vol. 2017, Iss. 1, pp. 148-201
Open Access | Times Cited: 65

Showing 1-25 of 65 citing articles:

Recent advances in the application of indoles in multicomponent reactions
Ghodsi Mohammadi Ziarani, Razieh Moradi, Tahereh Ahmadi, et al.
RSC Advances (2018) Vol. 8, Iss. 22, pp. 12069-12103
Open Access | Times Cited: 114
The application of isatin-based multicomponent-reactions in the quest for new bioactive and druglike molecules
Pedro Brandão, Carolina S. Marques, Anthony J. Burke, et al.
European Journal of Medicinal Chemistry (2020) Vol. 211, pp. 113102-113102
Open Access | Times Cited: 97
Isatin containing heterocycles for different biological activities: Analysis of structure activity relationship
Rajarshi Nath, Shelly Pathania, Gourav Grover, et al.
Journal of Molecular Structure (2020) Vol. 1222, pp. 128900-128900
Closed Access | Times Cited: 93
Visible‐Light‐Mediated Dearomatisation of Indoles and Pyrroles to Pharmaceuticals and Pesticides
Waldemar Schilling, Yu Zhang, D. D. Riemer, et al.
Chemistry - A European Journal (2019) Vol. 26, Iss. 2, pp. 390-395
Open Access | Times Cited: 81
Asymmetric synthesis of chiral oxindoles using isatin as starting material
Ghodsi Mohammadi Ziarani, Razieh Moradi, Negar Lashgari
Tetrahedron (2018) Vol. 74, Iss. 13, pp. 1323-1353
Closed Access | Times Cited: 65
Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, et al.
The Chemical Record (2021) Vol. 21, Iss. 4, pp. 924-1037
Open Access | Times Cited: 43
Stereoselective Synthesis of 3,3-Disubstituted Oxindoles and Spirooxindoles via Allylic Alkylation of Morita–Baylis–Hillman Carbonates of Isatins with Cyclic Sulfamidate Imines Catalyzed by DABCO
Sanjeeva K. Arupula, Soumitra Guin, Anubha Yadav, et al.
The Journal of Organic Chemistry (2018) Vol. 83, Iss. 5, pp. 2660-2675
Closed Access | Times Cited: 54
Skeletal Editing of Isatins for Heterocycle Molecular Diversity
Tiantian Zhang, Huangdi Feng
The Chemical Record (2024) Vol. 24, Iss. 6
Closed Access | Times Cited: 5
Isatin: A Scaffold with Immense Biodiversity
Priyobrata Nath, Agnish Mukherjee, Sougata Mukherjee, et al.
Mini-Reviews in Medicinal Chemistry (2020) Vol. 21, Iss. 9, pp. 1096-1112
Closed Access | Times Cited: 37
A novel Hg2+ ion chemosensor based on dihydro-pyrano imidazole derivatives
Ghodsi Mohammadi Ziarani, Nikoo Shamkhali, Zahra Panahande, et al.
Journal of Molecular Structure (2025) Vol. 1337, pp. 142096-142096
Closed Access
2-Aminophenones, a common precursor to N-aryl isatins and acridines endowed with bioactivities
Nahida Mokhtari Brikci-Nigassa, Ghenia Bentabed‐Ababsa, William Erb, et al.
Tetrahedron (2018) Vol. 74, Iss. 15, pp. 1785-1801
Open Access | Times Cited: 30
Ugi Reaction Synthesis of Oxindole–Lactam Hybrids as Selective Butyrylcholinesterase Inhibitors
Pedro Brandão, Óscar López, Luisa Leitzbach, et al.
ACS Medicinal Chemistry Letters (2021) Vol. 12, Iss. 11, pp. 1718-1725
Open Access | Times Cited: 21
Facile synthesis of isatins by direct oxidation of indoles and 3-iodoindoles using NIS/IBX
Ajeet Chandra, Navin Yadav, Jarugu Narasimha Moorthy
Tetrahedron (2019) Vol. 75, Iss. 14, pp. 2169-2174
Closed Access | Times Cited: 25
N-Heterocyclic carbene catalyzed chemo- and enantioselective cross-benzoin reaction of aldehydes with isatins
Jianfeng Xu, Jingyi Peng, Chonglong He, et al.
Organic Chemistry Frontiers (2018) Vol. 6, Iss. 2, pp. 172-176
Closed Access | Times Cited: 24
Review on Isatin- A Remarkable Scaffold for Designing Potential Therapeutic Complexes and Its Macrocyclic Complexes with Transition Metals
Swati Bugalia, Yogpal Dhayal, Harshita Sachdeva, et al.
Journal of Inorganic and Organometallic Polymers and Materials (2023) Vol. 33, Iss. 7, pp. 1782-1801
Open Access | Times Cited: 7
Synthesis of dispirocyclohexadiene bisoxindole from Morita-Baylis-Hillman carbonate of isatin
Beom Kyu Min, Sangku Lee, Hwa Jung Roh, et al.
Tetrahedron Letters (2017) Vol. 58, Iss. 33, pp. 3251-3255
Closed Access | Times Cited: 23
Isatin Derivatives Containing Sterically Hindered Phenolic Fragment and Water-Soluble Acyl Hydrazones on Their Basis: Synthesis and Antimicrobial Activity
А. В. Богданов, Ilyuza F. Zaripova, A. D. Voloshina, et al.
Russian Journal of General Chemistry (2018) Vol. 88, Iss. 1, pp. 57-67
Closed Access | Times Cited: 22
Synthesis and Reactivity of 3,3-Diazidooxindoles
Kristina Holzschneider, Fabian Mohr, Stefan F. Kirsch
Organic Letters (2018) Vol. 20, Iss. 22, pp. 7066-7070
Closed Access | Times Cited: 22
The molecular diversity scope of 4-hydroxycoumarin in the synthesis of heterocyclic compounds via multicomponent reactions
Ghodsi Mohammadi Ziarani, Razieh Moradi, Tahereh Ahmadi, et al.
Molecular Diversity (2019) Vol. 23, Iss. 4, pp. 1029-1064
Closed Access | Times Cited: 21
Graphene oxide-catalysed carbene-transfer reaction in water: a highly “green” and selective approach to access 3,3′,3′′-trisindoles
Priya Kamboj, Vikas Tyagi
Green Chemistry (2023) Vol. 26, Iss. 4, pp. 1990-1999
Closed Access | Times Cited: 6
Synthesis and Biological Evaluation of New Isatin‐Based QACs with High Antimicrobial Potency
А. В. Богданов, Ilyuza F. Zaripova, Alexandra D. Voloshina, et al.
ChemistrySelect (2019) Vol. 4, Iss. 20, pp. 6162-6166
Closed Access | Times Cited: 18
New cell cycle checkpoint pathways regulators with 2-Oxo-indoline scaffold as potential anticancer agents: Design, synthesis, biological activities and in silico studies
Hend A. A. Abd El-wahab, Hany S. Mansour, Ahmed M. Ali, et al.
Bioorganic Chemistry (2022) Vol. 120, pp. 105622-105622
Closed Access | Times Cited: 10
Synthesis of Heterocyclic Compounds Based on Isatins
Zahra Sadeghian, Mohammad Bayat
Current Organic Chemistry (2022) Vol. 26, Iss. 8, pp. 756-770
Closed Access | Times Cited: 10
Synthesis of Aryl Silacarboxylates via Palladium-Catalyzed C–O Bond Formation of Silacarboxylic Acids and Aryl Iodides
Jinyan Liang, Shou-Jie Shen, Xiao-Hu Xu, et al.
Organic Letters (2018) Vol. 20, Iss. 21, pp. 6627-6631
Closed Access | Times Cited: 18
BINOL derivatives-catalysed enantioselective allylboration of isatins: application to the synthesis of (R)-chimonamidine
Julien Braire, Vincent Dorcet, Joëlle Vidal, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 31, pp. 6042-6046
Open Access | Times Cited: 15
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