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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:

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

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
Donor–Acceptor Cyclopropanes as an Expedient Building Block Towards the Construction of Nitrogen‐Containing Molecules: An Update
Priyanka Singh, Rohit Kumar Varshnaya, Raghunath Dey, et al.
Advanced Synthesis & Catalysis (2019) Vol. 362, Iss. 7, pp. 1447-1484
Closed Access | Times Cited: 143
Recent Advances in the Construction of Trifluoromethyl‐Containing Spirooxindoles through Cycloaddition Reactions
Hou‐Ze Gui, Yin Wei, Min Shi
Chemistry - An Asian Journal (2020) Vol. 15, Iss. 8, pp. 1225-1233
Closed Access | Times Cited: 79
Ring‐Opening 1,3‐Aminochalcogenation of Donor–Acceptor Cyclopropanes: A Three‐Component Approach
André U. Augustin, Peter G. Jones, Daniel B. Werz
Chemistry - A European Journal (2019) Vol. 25, Iss. 50, pp. 11620-11624
Open Access | Times Cited: 62
Recent advances in ring-opening reactions of 2-substituted donor-acceptor cyclopropanes under metal catalysis
Fatemeh Doraghi, Somaye Karimian, Omid Hosseinchi Qareaghaj, et al.
Journal of Organometallic Chemistry (2023) Vol. 1005, pp. 122963-122963
Closed Access | Times Cited: 13
Cycloaddition and Annulation Reactions of Donor–Acceptor Cyclopropanes
Роман А. Новиков, Denis D. Borisov, Yury V. Tomilov
(2024), pp. 37-138
Closed Access | Times Cited: 4
Chemical transformations of 2-phenylcyclopropane-1,1-dinitrile under the action of Lewis acids
Denis D. Borisov, Daniil A. Knyazev, Роман А. Новиков, et al.
Mendeleev Communications (2025) Vol. 35, Iss. 1, pp. 93-95
Closed Access
The Therapeutic Potential of Spirooxindoles in Cancer: A Focus on p53–MDM2 Modulation
Adel S. Girgis, Yujun Zhao, Angel Nkosi, et al.
Pharmaceuticals (2025) Vol. 18, Iss. 2, pp. 274-274
Open Access
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
Ring-opening cyclization of spirocyclopropanes with stabilized sulfonium ylides for the construction of a chromane skeleton
Hisanori Nambu, Yuta Onuki, Naoki Ono, et al.
Chemical Communications (2019) Vol. 55, Iss. 46, pp. 6539-6542
Open Access | Times Cited: 21
Synthesis, Biological and In Silico Evaluation of Pure Nucleobase-Containing Spiro (Indane-Isoxazolidine) Derivatives as Potential Inhibitors of MDM2–p53 Interaction
Loredana Maiuolo, Vincenzo Algieri, Beatrice Russo, et al.
Molecules (2019) Vol. 24, Iss. 16, pp. 2909-2909
Open Access | Times Cited: 21
A Formal Condensation and [4+1] Annulation Reaction of 3‐Isothiocyanato Oxindoles with Aza‐o‐Quinone Methides
Hou‐Ze Gui, Xiao‐Yun Wu, Yin Wei, et al.
Advanced Synthesis & Catalysis (2019) Vol. 361, Iss. 23, pp. 5466-5471
Closed Access | Times Cited: 20
Catalytic asymmetric synthesis of 3,2′-pyrrolinyl spirooxindoles via conjugate addition/Schmidt-type rearrangement of vinyl azides and (E)-alkenyloxindoles
Ziwei Zhong, Zhijie Xiao, Xiaohua Liu, et al.
Chemical Science (2020) Vol. 11, Iss. 42, pp. 11492-11497
Open Access | Times Cited: 19
Chiral Brønsted Base Activation of Donor–Acceptor Cyclopropanes toward Diastereo- and Enantioselective [3 + 2] Cycloaddition with Isatin-Derived Ketimines
Zhe‐Jia Yu, Shuang Yan, Xiao‐Li Zhao, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 12, pp. 8691-8705
Closed Access | Times Cited: 2
Divergent Copper‐salt‐controlled Reactions of Donor‐Acceptor Cyclopropanes and N‐Fluorobenzene Sulfonimide: Access to the 1,3‐Haloamines and Aminoindanes
Lingyan Liu, Xiao Wang, Weiguo Xiao, et al.
Chemistry - A European Journal (2022) Vol. 29, Iss. 3
Closed Access | Times Cited: 10
Synthesis of functionalized 3,2′-pyrrolidinyl spirooxindoles via domino 1,6-addition/annulation reactions of para-quinone methides and 3-chlorooxindoles
Xiaochen Tian, Yongxing Zhang, Weiwu Ren, et al.
Organic Chemistry Frontiers (2021) Vol. 9, Iss. 3, pp. 615-626
Closed Access | Times Cited: 11
cis-Diastereoselective Synthesis of Spirooxindolo-β-Lactams by Staudinger Cycloaddition with TsCl as Activating Co-reagent
Vadim Filatov, Juliana Kuznetsova, Lada M. Petrovskaya, et al.
ACS Omega (2021) Vol. 6, Iss. 35, pp. 22740-22751
Open Access | Times Cited: 9
Lewis acid-catalyzed [4 + 2] cycloaddition of donor–acceptor cyclobutanes with iminooxindoles: access to spiro[piperidine-3,2′-oxindoles]
Zuliang Chen, Keyi Yan, Hui Luo, et al.
RSC Advances (2022) Vol. 12, Iss. 49, pp. 32097-32101
Open Access | Times Cited: 5
Lewis acid-catalyzed [3 + 2] annulations of oxindole based spirocyclic donor–acceptor cyclopropanes with ynamides
Dongxin Zhang, Qihang Cheng, Lvjia Chen, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 44, pp. 9645-9648
Closed Access | Times Cited: 7
Diastereoselectivity‐Switchable Gold‐Catalyzed Formal [3+2]‐Cycloadditions of N‐2,2,2‐Trifluoroethylisatin Ketimines with Yne−Enones
Jun‐An Xiao, Xiuliang Cheng, Hai Peng, et al.
Chemistry - An Asian Journal (2021) Vol. 16, Iss. 17, pp. 2435-2438
Closed Access | Times Cited: 6
From Enantioenriched Donor‐Acceptor Cyclopropylcarbinols to Axially Chiral Arylnaphthalenes through Aryldihydronaphthalenes: Central‐to‐Axial Chirality Exchange
Taichi Saito, Yuka Shimizu, Yusuke Araki, et al.
European Journal of Organic Chemistry (2021) Vol. 2022, Iss. 1
Open Access | Times Cited: 6
An ultrasound assisted synthesis of spirooxindolo-1,2,4-oxadiazoles via [3+2] cycloaddition reaction and their anti-cancer activity
Madhu Kanchrana, Bhargava Sai Allaka, Gamidi Rama Krishna, et al.
ARKIVOC (2023) Vol. 2023, Iss. 6
Open Access | Times Cited: 2
Take Advantage of the N‐Nucleophilicity of Imine in Catalytic Cyclization Reactions
Linqing Wang, Dongxu Yang
ChemCatChem (2023) Vol. 15, Iss. 9
Closed Access | Times Cited: 2
An iron-catalyzed domino reaction of donor–acceptor cyclopropanes: a diastereoselective approach towards diversely functionalized pyrrolo-quinazolines
Samiran Dhara, Subhadeep Ghosh, Asish R. Das
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 7, pp. 1415-1424
Closed Access | Times Cited: 3
Synthesis of (2-(Quinolin-2-yl)phenyl)carbamates by a One-Pot Friedel–Crafts Reaction/Oxidative Umpolung Aza-Grob Fragmentation Sequence
Dong Xie, Xin Xu, Sihui Long, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 12, pp. 7852-7863
Closed Access | Times Cited: 3
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