Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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 Functionalized 3-Spiro[cyclopropa[a]pyrrolizine]- and 3-Spiro[3-azabicyclo[3.1.0]hexane]oxindoles from Cyclopropenes and Azomethine Ylides via [3 + 2]-Cycloaddition
Alexander S. Filatov, Nickolay A. Knyazev, A. P. Molchanov, et al.
The Journal of Organic Chemistry (2016) Vol. 82, Iss. 2, pp. 959-975
Closed Access | Times Cited: 81

Showing 1-25 of 81 citing articles:

Recent advances in spirocyclization of indole derivatives
Jitender Bariwal, Leonid G. Voskressensky, Erik V. Van der Eycken
Chemical Society Reviews (2018) Vol. 47, Iss. 11, pp. 3831-3848
Open Access | Times Cited: 341
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
An overview of spirooxindole as a promising scaffold for novel drug discovery
Liming Zhou, Ren‐Yu Qu, Guang‐Fu Yang
Expert Opinion on Drug Discovery (2020) Vol. 15, Iss. 5, pp. 603-625
Closed Access | Times Cited: 229
Recent developments in cyclopropene chemistry
Penghua Li, Xiaoyu Zhang, Min Shi
Chemical Communications (2020) Vol. 56, Iss. 41, pp. 5457-5471
Closed Access | Times Cited: 94
Synthesis of bicyclo[3.1.0]hexanes by (3 + 2) annulation of cyclopropenes with aminocyclopropanes
Bastian Muriel, Alec Gagnebin, Jérôme Waser
Chemical Science (2019) Vol. 10, Iss. 46, pp. 10716-10722
Open Access | Times Cited: 81
Highly Efficient Synthesis of Spiro[1-azabicyclo[3.2.0]heptane] Frameworks via [3+2]-Cycloaddition
Yulia A. Pronina, Alexander S. Filatov, Stanislav V. Shmakov, et al.
The Journal of Organic Chemistry (2025)
Closed Access | Times Cited: 1
Recent Advances on Diverse Decarboxylative Reactions of Amino Acids
Matiur Rahman, Anindita Mukherjee, Igor S. Коvalev, et al.
Advanced Synthesis & Catalysis (2018) Vol. 361, Iss. 10, pp. 2161-2214
Closed Access | Times Cited: 82
Modern Trends of Organic Chemistry in Russian Universities
А. И. Коновалов, И. С. Антипин, В. А. Бурилов, et al.
Russian Journal of Organic Chemistry (2018) Vol. 54, Iss. 2, pp. 157-371
Closed Access | Times Cited: 77
Synthetic Applications of Cyclopropene and Cyclopropenone: Recent Progress and Developments
Bishnu Prasad Raiguru, Sabita Nayak, Deepak Ranjan Mishra, et al.
Asian Journal of Organic Chemistry (2020) Vol. 9, Iss. 8, pp. 1088-1132
Closed Access | Times Cited: 60
Recent advances in the (3+2) cycloaddition of azomethine ylide
Sapana Dubey, Anit Pal, S. R. Roy, et al.
New Journal of Chemistry (2023) Vol. 47, Iss. 19, pp. 8997-9034
Closed Access | Times Cited: 21
Diversity-Oriented Synthesis of Spiropyrrolo[1,2-a]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-Component 1,3-Dipolar Cycloaddition Reactions: In Vitro and in Vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues
Amani Toumi, Sarra Boudriga, Khaled Hamden, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 19, pp. 13420-13445
Closed Access | Times Cited: 35
A highly diastereoselective one-pot three-component 1,3-dipolar cycloaddition of cyclopropenes with azomethine ylides generated from 11H-indeno[1,2-b]-quinoxalin-11-ones
Alexander S. Filatov, Nickolay A. Knyazev, Mikhail N. Ryazantsev, et al.
Organic Chemistry Frontiers (2017) Vol. 5, Iss. 4, pp. 595-605
Closed Access | Times Cited: 43
Stereo- and Regioselective 1,3-Dipolar Cycloaddition of the Stable Ninhydrin-Derived Azomethine Ylide to Cyclopropenes: Trapping of Unstable Cyclopropene Dipolarophiles
Alexander S. Filatov, Siqi Wang, Olesya V. Khoroshilova, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 11, pp. 7017-7036
Closed Access | Times Cited: 42
Asymmetric Construction of 3-Azabicyclo[3.1.0]hexane Skeleton with Five Contiguous Stereogenic Centers by Cu-Catalyzed 1,3-Dipolar Cycloaddition of Trisubstituted Cyclopropenes
Hua Deng, Wu‐Lin Yang, Fei Tian, et al.
Organic Letters (2018) Vol. 20, Iss. 13, pp. 4121-4125
Closed Access | Times Cited: 41
Concise Synthesis of Tryptanthrin Spiro Analogues with In Vitro Antitumor Activity Based on One-Pot, Three-Component 1,3-Dipolar Cycloaddition of Azomethine Ylides to Сyclopropenes
Vitaly M. Boitsov, Alexander V. Stepakov, Alexander S. Filatov, et al.
Synthesis (2018) Vol. 51, Iss. 03, pp. 713-729
Closed Access | Times Cited: 38
Construction of heterocyclic rings from cyclopropenes
Hengrui Huo, Yuefa Gong
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 19, pp. 3847-3869
Closed Access | Times Cited: 22
Cyclopropenes and methylenecyclopropanes in 1,3-dipolar cycloaddition reactions
А. П. Молчанов, Мария М. Ефремова, Михаил А. Кузнецов
Russian Chemical Bulletin (2022) Vol. 71, Iss. 4, pp. 620-650
Closed Access | Times Cited: 19
1-Styryl-1,3-diketones in the synthesis of spiro[oxindole-3,2′-pyrrolidines] with notable anticancer activity
Nikolay S. Zimnitskiy, Vladislav Yu. Korotaev, Maria V. Ulitko, et al.
Molecular Diversity (2025)
Closed Access
Microwave‐Assisted One‐Pot [3+2] Cycloaddition of Azomethine Ylides and 3‐Alkenyl Oxindoles: A Facile Approach to Pyrrolidine‐Fused Bis‐Spirooxindoles
Sonal Bhandari, Sravani Sana, Balasubramanyam Sridhar, et al.
ChemistrySelect (2019) Vol. 4, Iss. 5, pp. 1727-1730
Closed Access | Times Cited: 35
1,3-Dipolar Cycloaddition of Isatin-Derived Azomethine Ylides with 2H-Azirines: Stereoselective Synthesis of 1,3-Diazaspiro[bicyclo[3.1.0]hexane]oxindoles
Anikó Angyal, András Demjén, Veronika Harmat, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 7, pp. 4273-4281
Open Access | Times Cited: 31
Dipolarophile-Controlled Regioselective 1,3-Dipolar Cycloaddition: A Switchable Divergent Access to Functionalized N-Fused Pyrrolidinyl Spirooxindoles
Yongchao Wang, Lijun Yan, Yu‐Xin Yan, et al.
International Journal of Molecular Sciences (2023) Vol. 24, Iss. 4, pp. 3771-3771
Open Access | Times Cited: 9
Decarboxylative 1,3-dipolar cycloadditions of l-proline
Fatemeh Doraghi, Azam Serajian, Somaye Karimian, et al.
RSC Advances (2024) Vol. 14, Iss. 12, pp. 8481-8501
Open Access | Times Cited: 3
A copper-catalyzed reaction of 3-diazoindolin-2-imines with 2-(phenylamino)ethanols: convenient access to spiro[indoline-3,2′-oxazolidin]-2-imines
Guorong Sheng, Shicong Ma, Songlin Bai, et al.
Chemical Communications (2018) Vol. 54, Iss. 12, pp. 1529-1532
Closed Access | Times Cited: 28
An Efficient Synthesis of Oxygen-Bridged Spirooxindoles via Microwave-Promoted Multicomponent Reaction
Yaojing Shi, Hua Zhao, Yufen Zhao
Molecules (2023) Vol. 28, Iss. 8, pp. 3508-3508
Open Access | Times Cited: 8
Benzylarylation of N-Allyl Anilines: Synthesis of Benzylated Indolines
Wenzhong Huang, Xiulan Li, Xuemei Song, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 10, pp. 6072-6083
Closed Access | Times Cited: 25
Page 1 - Next Page

Scroll to top