
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:
Synthesis of indoles: recent advances
Dmitry I. Bugaenko, Alexander V. Karchava, M. A. Yurovskaya
Russian Chemical Reviews (2018) Vol. 88, Iss. 2, pp. 99-159
Closed Access | Times Cited: 74
Dmitry I. Bugaenko, Alexander V. Karchava, M. A. Yurovskaya
Russian Chemical Reviews (2018) Vol. 88, Iss. 2, pp. 99-159
Closed Access | Times Cited: 74
Showing 1-25 of 74 citing articles:
Visible light-mediated chemistry of indoles and related heterocycles
Alexey А. Festa, Leonid G. Voskressensky, Erik V. Van der Eycken
Chemical Society Reviews (2019) Vol. 48, Iss. 16, pp. 4401-4423
Closed Access | Times Cited: 259
Alexey А. Festa, Leonid G. Voskressensky, Erik V. Van der Eycken
Chemical Society Reviews (2019) Vol. 48, Iss. 16, pp. 4401-4423
Closed Access | Times Cited: 259
Ketones as strategic building blocks for the synthesis of natural product-inspired compounds
Daniel J. Foley, Herbert Waldmann
Chemical Society Reviews (2022) Vol. 51, Iss. 10, pp. 4094-4120
Closed Access | Times Cited: 79
Daniel J. Foley, Herbert Waldmann
Chemical Society Reviews (2022) Vol. 51, Iss. 10, pp. 4094-4120
Closed Access | Times Cited: 79
An insight into the advanced synthetic recipes to access ubiquitous indole heterocycles
Basavarajaiah Suliphuldevara Mathada, Nagesh Gunavanthrao Yernale, N. Jeelan Basha, et al.
Tetrahedron Letters (2021) Vol. 85, pp. 153458-153458
Closed Access | Times Cited: 58
Basavarajaiah Suliphuldevara Mathada, Nagesh Gunavanthrao Yernale, N. Jeelan Basha, et al.
Tetrahedron Letters (2021) Vol. 85, pp. 153458-153458
Closed Access | Times Cited: 58
One-Pot Synthesis of 1,2,3-Triarylindoles through Cascade Reactions Using Calcium Carbide, Iodoarenes, and Aromatic Amines
Zhenrong Liu, Zhiqiang Wang, Liao Haiyan, et al.
Organic Letters (2023) Vol. 25, Iss. 31, pp. 5812-5816
Closed Access | Times Cited: 18
Zhenrong Liu, Zhiqiang Wang, Liao Haiyan, et al.
Organic Letters (2023) Vol. 25, Iss. 31, pp. 5812-5816
Closed Access | Times Cited: 18
Small-molecule fluorogenic probes based on indole scaffold
Pintu Ghosh, Anirban Karak, Ajit Kumar Mahapatra
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 14, pp. 2690-2718
Closed Access | Times Cited: 8
Pintu Ghosh, Anirban Karak, Ajit Kumar Mahapatra
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 14, pp. 2690-2718
Closed Access | Times Cited: 8
(Indol-3-yl)(DMIX)Iodonium Salts: Novel Electrophilic Indole Reagents
Dmitry I. Bugaenko, Nikolai A. Malashchenko, Sergei O. Kopytov, et al.
Organic Letters (2024) Vol. 26, Iss. 15, pp. 3189-3194
Closed Access | Times Cited: 7
Dmitry I. Bugaenko, Nikolai A. Malashchenko, Sergei O. Kopytov, et al.
Organic Letters (2024) Vol. 26, Iss. 15, pp. 3189-3194
Closed Access | Times Cited: 7
Indole: A promising scaffold for the discovery and development of potential anti-tubercular agents
Nilesh Gajanan Bajad, Sudhir Kumar Singh, Sushil Kumar Singh, et al.
Current Research in Pharmacology and Drug Discovery (2022) Vol. 3, pp. 100119-100119
Open Access | Times Cited: 26
Nilesh Gajanan Bajad, Sudhir Kumar Singh, Sushil Kumar Singh, et al.
Current Research in Pharmacology and Drug Discovery (2022) Vol. 3, pp. 100119-100119
Open Access | Times Cited: 26
Synthesis, biological evaluation, molecular docking, and DFT calculation of novel 4-(1H-indol-3-yl)-3-methyl-1-phenyl-1H-furo[2,3-c]pyrazole derivatives
Mahmoud Nassiri, Jaber Salehzadeh, Sahar Mohajeri
Results in Chemistry (2025), pp. 102074-102074
Open Access
Mahmoud Nassiri, Jaber Salehzadeh, Sahar Mohajeri
Results in Chemistry (2025), pp. 102074-102074
Open Access
Indoles in Drug Design and Medicinal Chemistry
Benjamin Ayodipupo Babalola, Monika Malik, Olanike Olowokere, et al.
European Journal of Medicinal Chemistry Reports (2025), pp. 100252-100252
Open Access
Benjamin Ayodipupo Babalola, Monika Malik, Olanike Olowokere, et al.
European Journal of Medicinal Chemistry Reports (2025), pp. 100252-100252
Open Access
Synthesis of 1,2-Disubstituted-3-thioindoles by the Madelung Reaction
G. K. Sterligov, Maria A. Rasskazova, Maxim A. Topchiy, et al.
Russian Journal of Organic Chemistry (2025) Vol. 61, Iss. 2, pp. 217-224
Closed Access
G. K. Sterligov, Maria A. Rasskazova, Maxim A. Topchiy, et al.
Russian Journal of Organic Chemistry (2025) Vol. 61, Iss. 2, pp. 217-224
Closed Access
Recent advances in catalytic approaches for the synthesis of 3-substituted indoles: mechanisms and strategies
Ebraheem Abdu Musad Saleh, Kakul Hussin Firoz, Subasini Uthirapathy, et al.
RSC Advances (2025) Vol. 15, Iss. 16, pp. 12255-12290
Open Access
Ebraheem Abdu Musad Saleh, Kakul Hussin Firoz, Subasini Uthirapathy, et al.
RSC Advances (2025) Vol. 15, Iss. 16, pp. 12255-12290
Open Access
Micellar nanoreactors for organic transformations with a focus on “dehydration” reactions in water: A decade update
Mainak Banerjee, Padmini C. Panjikar, Zigmee T. Bhutia, et al.
Tetrahedron (2021) Vol. 88, pp. 132142-132142
Closed Access | Times Cited: 26
Mainak Banerjee, Padmini C. Panjikar, Zigmee T. Bhutia, et al.
Tetrahedron (2021) Vol. 88, pp. 132142-132142
Closed Access | Times Cited: 26
Catalytic Enantioselective Desymmetrizing Fischer Indolization through Dynamic Kinetic Resolution
Biki Ghosh, Reena Balhara, Garima Jindal, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 16, pp. 9086-9092
Closed Access | Times Cited: 25
Biki Ghosh, Reena Balhara, Garima Jindal, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 16, pp. 9086-9092
Closed Access | Times Cited: 25
A Minireview on the Scope of Cadogan Cyclization Reactions Leading to Diverse Azaheterocycles
Manpreet Kaur, Raj Kumar
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 6
Closed Access | Times Cited: 18
Manpreet Kaur, Raj Kumar
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 6
Closed Access | Times Cited: 18
Indole frameworks via transition-metal-free annulation: a current perspective
Suven Das
New Journal of Chemistry (2023) Vol. 47, Iss. 29, pp. 13729-13775
Closed Access | Times Cited: 10
Suven Das
New Journal of Chemistry (2023) Vol. 47, Iss. 29, pp. 13729-13775
Closed Access | Times Cited: 10
Carbonylative synthesis and functionalization of indoles
Alex De Salvo, Raffaella Mancuso, Xiao‐Feng Wu
Beilstein Journal of Organic Chemistry (2024) Vol. 20, pp. 973-1000
Open Access | Times Cited: 3
Alex De Salvo, Raffaella Mancuso, Xiao‐Feng Wu
Beilstein Journal of Organic Chemistry (2024) Vol. 20, pp. 973-1000
Open Access | Times Cited: 3
Palladium-Catalyzed Sequential C–H Activation/Amination with Diaziridinone: An Approach to Indoles
Jing Li, Jinhua Chen, Luying Wang, et al.
Organic Letters (2021) Vol. 23, Iss. 9, pp. 3646-3651
Closed Access | Times Cited: 23
Jing Li, Jinhua Chen, Luying Wang, et al.
Organic Letters (2021) Vol. 23, Iss. 9, pp. 3646-3651
Closed Access | Times Cited: 23
Domino C–N Bond Formation via a Palladacycle with Diaziridinone. An Approach to Indolo[3,2-b]indoles
Sudarshan Debnath, Lingli Liang, Mei Lü, et al.
Organic Letters (2021) Vol. 23, Iss. 9, pp. 3237-3242
Closed Access | Times Cited: 21
Sudarshan Debnath, Lingli Liang, Mei Lü, et al.
Organic Letters (2021) Vol. 23, Iss. 9, pp. 3237-3242
Closed Access | Times Cited: 21
Grindstone chemistry: A “green” approach for the synthesis and derivatization of heterocycles
Mainak Banerjee, Padmini C. Panjikar, Dharmendra Das, et al.
Tetrahedron (2022) Vol. 112, pp. 132753-132753
Closed Access | Times Cited: 15
Mainak Banerjee, Padmini C. Panjikar, Dharmendra Das, et al.
Tetrahedron (2022) Vol. 112, pp. 132753-132753
Closed Access | Times Cited: 15
Generation of aryl radicals by redox processes. Recent progress in the arylation methodology
Dmitry I. Bugaenko, Alexey A. Volkov, Alexander V. Karchava, et al.
Russian Chemical Reviews (2020) Vol. 90, Iss. 1, pp. 116-170
Closed Access | Times Cited: 20
Dmitry I. Bugaenko, Alexey A. Volkov, Alexander V. Karchava, et al.
Russian Chemical Reviews (2020) Vol. 90, Iss. 1, pp. 116-170
Closed Access | Times Cited: 20
Electrochemical [3+2] Cycloaddition of Anilines and 1,3‐Dicarbonyl Compounds: Construction of Multisubstituted Indoles
Xiaoqiang Chang, Nanjun Chen, Sixian Lu, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 16, pp. 2865-2871
Closed Access | Times Cited: 12
Xiaoqiang Chang, Nanjun Chen, Sixian Lu, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 16, pp. 2865-2871
Closed Access | Times Cited: 12
Annulation of 2‐Alkynylanilines: The Versatile Chemical Compounds
Vaezeh Fathi Vavsari, Ali M. Nikbakht, Saeed Balalaie
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 2
Closed Access | Times Cited: 11
Vaezeh Fathi Vavsari, Ali M. Nikbakht, Saeed Balalaie
Asian Journal of Organic Chemistry (2022) Vol. 11, Iss. 2
Closed Access | Times Cited: 11
Pd(II)‐Catalyzed [3+2] Annulation of N‐Aryl‐2‐aminopyridines and Alkynes toward N‐(2‐Pyridyl)indoles
Wenting Guo, Weiming Hu, Xinyu Zhang, et al.
Asian Journal of Organic Chemistry (2024) Vol. 13, Iss. 4
Closed Access | Times Cited: 2
Wenting Guo, Weiming Hu, Xinyu Zhang, et al.
Asian Journal of Organic Chemistry (2024) Vol. 13, Iss. 4
Closed Access | Times Cited: 2
Transition‐Metal‐Free Synthesis of 1,2‐Disubstituted Indoles
Gleb A. Chesnokov, Alexandra A. Ageshina, Maxim A. Topchiy, et al.
European Journal of Organic Chemistry (2019) Vol. 2019, Iss. 30, pp. 4844-4854
Closed Access | Times Cited: 17
Gleb A. Chesnokov, Alexandra A. Ageshina, Maxim A. Topchiy, et al.
European Journal of Organic Chemistry (2019) Vol. 2019, Iss. 30, pp. 4844-4854
Closed Access | Times Cited: 17
Nitromethane as a reagent for the synthesis of 3-nitroindoles from 2-haloarylamine derivatives
Gleb A. Chesnokov, Alexandra A. Ageshina, A. V. Maryanova, et al.
Russian Chemical Bulletin (2020) Vol. 69, Iss. 12, pp. 2370-2377
Closed Access | Times Cited: 15
Gleb A. Chesnokov, Alexandra A. Ageshina, A. V. Maryanova, et al.
Russian Chemical Bulletin (2020) Vol. 69, Iss. 12, pp. 2370-2377
Closed Access | Times Cited: 15