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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:

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

Showing 1-25 of 27 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: 255
Exploiting Heavier Organochalcogen Compounds in Donor–Acceptor Cyclopropane Chemistry
André U. Augustin, Daniel B. Werz
Accounts of Chemical Research (2021) Vol. 54, Iss. 6, pp. 1528-1541
Closed Access | Times Cited: 130
Propagative isatin in organic synthesis of spirooxindoles through catalysis
Mohd Asif, Tazeen Azaz, Bhoopendra Tiwari, et al.
Tetrahedron (2023) Vol. 134, pp. 133308-133308
Closed Access | Times Cited: 28
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
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
Palladium-Catalyzed Annulative Coupling of Spirovinylcyclopropyl Oxindoles with p-Quinone Methides
Bijoy Debnath, Tanumay Sarkar, Pallab Karjee, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 14, pp. 9704-9719
Closed Access | Times Cited: 8
Enantioselective formal [3+2]-cycloadditions to access spirooxindoles bearing four contiguous stereocenters through synergistic catalysis
Jun‐An Xiao, Jinlian Li, Xiuliang Cheng, et al.
Chemical Communications (2021) Vol. 57, Iss. 36, pp. 4456-4459
Closed Access | Times Cited: 19
Metal-Free Regioselective Hydrophosphorodithioation of Spirovinylcyclopropyl Oxindoles: Rapid Access to Allyl Dialkylphosphorodithioates
Jiahua Wang, Fang Han, Siyuan Hao, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 19, pp. 12844-12853
Closed Access | Times Cited: 13
Imidazol-5-one as an Acceptor in Donor–Acceptor Cyclopropanes: Cycloaddition with Aldehydes
Andrey А. Mikhaylov, Андрей В. Кулешов, Pavel N. Solyev, et al.
Organic Letters (2020) Vol. 22, Iss. 7, pp. 2740-2745
Closed Access | Times Cited: 20
Anticancer potential of spirooxindole derivatives
Mohd Faiyyaz, Akanksha Tiwari, Saud Nusrat Ali, et al.
Elsevier eBooks (2024), pp. 605-619
Closed Access | Times Cited: 2
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
Reactions of Styrylmalonates with Aromatic Aldehydes: Detailed Synthetic and Mechanistic Studies
Denis D. Borisov, Роман А. Новиков, Yury V. Tomilov
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 6, pp. 4457-4471
Closed Access | Times Cited: 13
A simple method for the synthesis of isoindoline derivatives
Vitaly V. Shorokhov, Danyla S. Lebedev, Maksim А. Boichenko, et al.
Chemistry of Heterocyclic Compounds (2023) Vol. 59, Iss. 1-2, pp. 54-62
Closed Access | Times Cited: 5
Lewis‐Acid‐Catalyzed (3+2)‐Cycloadditions of Donor‐Acceptor Cyclopropanes with Thioketenes
Grzegorz Mlostoń, Mateusz Kowalczyk, André U. Augustin, et al.
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 46, pp. 6250-6253
Open Access | Times Cited: 12
Donor–Acceptor Bicyclopropyls as 1,6-Zwitterionic Intermediates: Synthesis and Reactions with 4-Phenyl-1,2,4-triazoline-3,5-dione and Terminal Acetylenes
Konstantin V. Potapov, Dmitry A. Denisov, Valeriia V. Glushkova, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 23, pp. 15562-15576
Closed Access | Times Cited: 12
Reversal of regioselectivity in reactions of donor–acceptor cyclopropanes with electrophilic olefins
Joanna Turkowska, Jakub Durka, Michał Ociepa, et al.
Chemical Communications (2021) Vol. 58, Iss. 4, pp. 509-512
Closed Access | Times Cited: 11
Ring-Opening/Recyclization Cascades of Monoactivated Cyclopropanes
Uttam K. Mishra, Kaushalendra Patel, S. S. V. Ramasastry
Organic Letters (2020) Vol. 22, Iss. 10, pp. 3815-3819
Closed Access | Times Cited: 11
Ambident reactivity of 5-aminopyrazoles towards donor–acceptor cyclopropanes
Anna E. Vartanova, Ирина И. Левина, Нина К. Ратманова, et al.
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 39, pp. 7795-7802
Closed Access | Times Cited: 7
Synthesis of 1,5-Substituted Pyrrolidin-2-ones from Donor–Acceptor Cyclopropanes and Anilines/Benzylamines
Maksim А. Boichenko, Andrey Yu. Plodukhin, Vitaly V. Shorokhov, et al.
Molecules (2022) Vol. 27, Iss. 23, pp. 8468-8468
Open Access | Times Cited: 7
Lewis Acid‐Catalyzed Formal (4+2)‐ and (2+2+2)‐Cycloaddition Between 1‐Azadienes and Styrylmalonates as Analogues of Donor‐Acceptor Cyclopropanes
Pavel G. Sergeev, Роман А. Новиков, Yury V. Tomilov
Advanced Synthesis & Catalysis (2021) Vol. 363, Iss. 23, pp. 5292-5299
Closed Access | Times Cited: 8
Additive‐Free Synthesis of Trifluoromethylated Spiro Cyclopropanes and Their Transformation into Trifluoromethylated Building Blocks
Anuj Kumar, Muhammad Fahad Jamali, Shilpa Thomas, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 6, pp. 1536-1541
Closed Access | Times Cited: 6
Concise approach to γ-(het)aryl- and γ-alkenyl-γ-aminobutyric acids. Synthesis of vigabatrin
Andrey Yu. Plodukhin, Maksim А. Boichenko, Иван А. Андреев, et al.
Organic & Biomolecular Chemistry (2023) Vol. 22, Iss. 5, pp. 1027-1033
Closed Access | Times Cited: 2
Donor-acceptor bicyclopropyl configuration-fixed by an additional trimethylene bridge: synthesis and Lewis acid-catalyzed tandem three-membered rings opening
Dmitry A. Denisov, Роман А. Новиков, Yury V. Tomilov
Russian Chemical Bulletin (2021) Vol. 70, Iss. 8, pp. 1568-1574
Closed Access | Times Cited: 5
Nucleophilic ring opening of imidazolone activated donor–acceptor cyclopropanes with alcohols
Viktoria А. Ikonnikova, Ekaterina A. Zhigileva, Андрей В. Кулешов, et al.
Mendeleev Communications (2021) Vol. 31, Iss. 5, pp. 657-658
Closed Access | Times Cited: 5
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