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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:

3-(2-Azidoethyl)oxindoles: Advanced Building Blocks for One-Pot Assembly of Spiro[pyrrolidine-3,3′-oxindoles]
Andrey A. Akaev, Elena V. Villemson, Nataliya S. Vorobyeva, et al.
The Journal of Organic Chemistry (2017) Vol. 82, Iss. 11, pp. 5689-5701
Closed Access | Times Cited: 37

Showing 1-25 of 37 citing articles:

Stereoselective synthesis and applications of spirocyclic oxindoles
Alexander J. Boddy, James A. Bull
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 5, pp. 1026-1084
Open Access | Times Cited: 253
Tandem construction of biological relevant aliphatic 5-membered N-heterocycles
Daniel Łowicki, Piotr Przybylski
European Journal of Medicinal Chemistry (2022) Vol. 235, pp. 114303-114303
Closed Access | Times Cited: 42
Syntheses and Applications of Spirocyclopropyl Oxindoles: A Decade Review
Akash P. Sakla, Pritish Kansal, Nagula Shankaraiah
European Journal of Organic Chemistry (2020) Vol. 2021, Iss. 5, pp. 757-772
Closed Access | Times Cited: 64
Efficient Synthesis of Spirooxindole Pyrrolones by a Rhodium(III)‐Catalyzed C−H Activation/Carbene Insertion/Lossen Rearrangement Sequence
Biao Ma, Peng Wu, Xing Wang, et al.
Angewandte Chemie International Edition (2019) Vol. 58, Iss. 38, pp. 13335-13339
Closed Access | Times Cited: 57
Domino Corey–Chaykovsky Reaction for One-Pot Access to Spirocyclopropyl Oxindoles
Saumen Hajra, Sayan Roy, SK Abu Saleh
Organic Letters (2018) Vol. 20, Iss. 15, pp. 4540-4544
Closed Access | Times Cited: 49
Recent Advances in Stereoselective Ring Expansion of Spirocyclopropanes: Access to the Spirocyclic Compounds
Tanumay Sarkar, Bijay Ketan Das, Kangkan Talukdar, et al.
ACS Omega (2020) Vol. 5, Iss. 41, pp. 26316-26328
Open Access | Times Cited: 42
Synthesis of Heterocycles from Donor-Acceptor Cyclopropanes: A Five-Year Recap
Ani Deepthi, C.B. Meenakshy, Maneesh Mohan
Synthesis (2023) Vol. 55, Iss. 23, pp. 3875-3894
Closed Access | Times Cited: 14
Mechanistic Study on the Asymmetric Cascade Michael Addition of Alkynone and Oxindole Catalyzed by Chiral Guanidine
Haoze Li, Cefei Zhang, Changwei Hu, et al.
The Journal of Organic Chemistry (2025)
Closed Access
Donor–acceptor cyclopropanes as ortho-quinone methide equivalents in formal (4 + 2)-cycloaddition to alkenes
Konstantin L. Ivanov, Stanislav I. Bezzubov, Mikhail Ya. Melnikov, et al.
Organic & Biomolecular Chemistry (2018) Vol. 16, Iss. 21, pp. 3897-3909
Closed Access | Times Cited: 35
Microwave‐Assisted Domino Palladium Catalysis in Water: A Diverse Synthesis of 3,3′‐Disubstituted Heterocyclic Compounds
Karu Ramesh, Basuli Suchand, Gedu Satyanarayana
European Journal of Organic Chemistry (2018) Vol. 2018, Iss. 19, pp. 2171-2177
Closed Access | Times Cited: 32
Nucleophilic Ring Opening of Donor–Acceptor Cyclopropanes with the Cyanate Ion: Access to Spiro[pyrrolidone-3,3′-oxindoles]
Sergey V. Zaytsev, Konstantin L. Ivanov, Dmitry A. Skvortsov, et al.
The Journal of Organic Chemistry (2018) Vol. 83, Iss. 15, pp. 8695-8709
Closed Access | Times Cited: 32
Lewis acid catalyzed annulation of spirocyclic donor–acceptor cyclopropanes with exo-heterocyclic olefins: access to highly functionalized bis-spirocyclopentane oxindole frameworks
Kuldeep Singh, Sourav Pramanik, Trevor A. Hamlin, et al.
Chemical Communications (2019) Vol. 55, Iss. 49, pp. 7069-7072
Open Access | Times Cited: 31
Ring Opening of Donor–Acceptor Cyclopropanes with Cyanide Ion and Its Surrogates
Maksim А. Boichenko, Иван А. Андреев, Alexey O. Chagarovskiy, et al.
The Journal of Organic Chemistry (2019) Vol. 85, Iss. 2, pp. 1146-1157
Closed Access | Times Cited: 28
Stereocontrolled [3+2] Cycloaddition of Donor–Acceptor Cyclopropanes to Iminooxindoles: Access to Spiro[oxindole-3,2′-pyrrolidines]
Andrey A. Akaev, Stanislav I. Bezzubov, Victor G. Desyatkin, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 6, pp. 3340-3356
Closed Access | Times Cited: 27
Chameleon-Like Activating Nature of the Spirooxindole Group in Donor–Acceptor Cyclopropanes
Andrey A. Akaev, Mikhail Ya. Melnikov, Екатерина М. Будынина
Organic Letters (2019) Vol. 21, Iss. 23, pp. 9795-9799
Closed Access | Times Cited: 27
aza-Wittig Reaction with Nitriles: How Carbonyl Function Switches from Reacting to Activating
Hamidulla B. Tukhtaev, Konstantin L. Ivanov, Stanislav I. Bezzubov, et al.
Organic Letters (2019) Vol. 21, Iss. 4, pp. 1087-1092
Closed Access | Times Cited: 26
Recent Advances in the Synthesis of Heterocycles by the Aza-Wittig Reaction
Mohammad Mahdavi, Keyvan Pedrood, Mohammad Nazari Montazer, et al.
Synthesis (2021) Vol. 53, Iss. 14, pp. 2342-2366
Closed Access | Times Cited: 23
Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone–cyclopropane-oxindoles bearing two vicinal spiro quaternary centers
Shengzheng Wang, Zhongjie Guo, Ying Wu, et al.
Organic Chemistry Frontiers (2019) Vol. 6, Iss. 9, pp. 1442-1447
Closed Access | Times Cited: 23
The Molecular Diversity Scope of Oxindole Derivatives in Organic Synthesis
Ghodsi Mohammadi Ziarani, Fatemeh Javadi, Fatemeh Mohajer
Current Organic Chemistry (2021) Vol. 25, Iss. 7, pp. 779-818
Closed Access | Times Cited: 16
Selective C3-Allylation and Formal [3 + 2]-Annulation of Spiro-Aziridine Oxindoles: Synthesis of 5′-Substituted Spiro[pyrrolidine-3,3′-oxindoles] and Coerulescine
SK Abu Saleh, Atanu Hazra, Maya Shankar Singh, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 13, pp. 8656-8671
Closed Access | Times Cited: 12
4‐(Dimethylamino)Pyridinium Azide in Protic Ionic Liquid Media as a Stable Equivalent of Hydrazoic Acid
Иван А. Андреев, Maksim А. Boichenko, Нина К. Ратманова, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 14, pp. 2403-2415
Closed Access | Times Cited: 11
Bi-Catalyzed 1,2-Reactivity of Spirocyclopropyl Oxindoles with Dithianediol: Access to Spiroheterocycles
Subhradeep Kar, Tanumay Sarkar, Prabhat Kumar Maharana, et al.
Organic Letters (2022) Vol. 24, Iss. 27, pp. 4965-4970
Closed Access | Times Cited: 11
New efficient synthesis of 1H-imidazo-[4,5-c]quinolines by a sequential Van Leusen/Staudinger/aza-Wittig/carbodiimide-mediated cyclization
Zhi‐Rong Guan, Zi-Ming Liu, Ming‐Wu Ding
Tetrahedron (2018) Vol. 74, Iss. 50, pp. 7186-7192
Closed Access | Times Cited: 15
Total synthesis of exigurin: the Ugi reaction in a hypothetical biosynthesis of natural products
Seijiro Hosokawa, Keisuke Nakanishi, Yutaro Udagawa, et al.
Organic & Biomolecular Chemistry (2019) Vol. 18, Iss. 4, pp. 687-693
Closed Access | Times Cited: 15
Convenient approach to polyoxygenated dibenzo[c,e]pyrrolo[1,2-a]azepines from donor–acceptor cyclopropanes
Maksim А. Boichenko, Оlga А. Ivanova, Иван А. Андреев, et al.
Organic Chemistry Frontiers (2018) Vol. 5, Iss. 19, pp. 2829-2834
Closed Access | Times Cited: 13
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