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:

Showing 1-25 of 34 citing articles:

Diastereo- and Enantioselective Construction of 3,3′-Pyrrolidinyldispirooxindole Framework via Catalytic Asymmetric 1,3-Dipolar Cycloadditions
Wei‐Min Dai, Xiaoli Jiang, Qiong Wu, et al.
The Journal of Organic Chemistry (2015) Vol. 80, Iss. 11, pp. 5737-5744
Closed Access | Times Cited: 168
Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction
Soukaina El Haddad, Sarra Boudriga, François Porzio, et al.
The Journal of Organic Chemistry (2015) Vol. 80, Iss. 18, pp. 9064-9075
Closed Access | Times Cited: 82
Organocatalytic asymmetric [3+2] cycloaddition of N-2,2,2-trifluoroethylisatin ketimines with 3-alkenyl-5-arylfuran-2(3H)-ones
Zhen‐Hua Wang, Zhijun Wu, Deng‐Feng Yue, et al.
Chemical Communications (2016) Vol. 52, Iss. 78, pp. 11708-11711
Closed Access | Times Cited: 82
Asymmetric synthesis of trifluoromethyl-substituted 3,3′-pyrrolidinyl-dispirooxindoles through organocatalytic 1,3-dipolar cycloaddition reactions
Wei-Jie Huang, Qing Chen, Ning Lin, et al.
Organic Chemistry Frontiers (2016) Vol. 4, Iss. 3, pp. 472-482
Closed Access | Times Cited: 77
Asymmetric synthesis of 3,3′-pyrrolidinyl-dispirooxindoles via a one-pot organocatalytic Mannich/deprotection/aza-Michael sequence
Kun Zhao, Ying Zhi, Xinyi Li, et al.
Chemical Communications (2015) Vol. 52, Iss. 11, pp. 2249-2252
Closed Access | Times Cited: 76
Design and synthesis of new substituted spirooxindoles as potential inhibitors of the MDM2–p53 interaction
Assem Barakat, Mohammad Shahidul Islam, Hussien Mansur Ghawas, et al.
Bioorganic Chemistry (2019) Vol. 86, pp. 598-608
Closed Access | Times Cited: 73
Asymmetric [3+2] Annulations to Construct 1,2‐Bispirooxindoles Incorporating a Dihydropyrrolidine Motif
Qing He, Wei Du, Ying‐Chun Chen
Advanced Synthesis & Catalysis (2017) Vol. 359, Iss. 21, pp. 3782-3791
Closed Access | Times Cited: 54
Regio- and stereoselective synthesis of new spirooxindoles via 1,3-dipolar cycloaddition reaction: Anticancer and molecular docking studies
Gehad Lotfy, El Sayed H. El Ashry, Mohamed M. Said, et al.
Journal of Photochemistry and Photobiology B Biology (2018) Vol. 180, pp. 98-108
Closed Access | Times Cited: 46
Design of novel dispirooxindolopyrrolidine and dispirooxindolopyrrolothiazole derivatives as potential antitubercular agents
Chourouk Mhiri, Sarra Boudriga, Moheddine Askri, et al.
Bioorganic & Medicinal Chemistry Letters (2015) Vol. 25, Iss. 19, pp. 4308-4313
Closed Access | Times Cited: 42
Diastereodivergent construction of bispiro[oxindole-bi-pyrrolidine]s with four consecutive stereocentersviaasymmetric [3 + 2] cycloaddition of 2,3-dioxopyrrolidines using identical catalysts
Xiaoyun Zhao, Jiale Xiong, Junkai An, et al.
Organic Chemistry Frontiers (2019) Vol. 6, Iss. 12, pp. 1989-1995
Closed Access | Times Cited: 42
A DBU-catalyzed Michael–Pinner–isomerization cascade reaction of 3-hydroxyoxindoles with isatylidene malononitriles: access to highly functionalized bispirooxindoles containing a fully substituted dihydrofuran motif
Yan‐Shuo Zhu, Wenbo Wang, Bei-Bei Yuan, et al.
Organic & Biomolecular Chemistry (2016) Vol. 15, Iss. 4, pp. 984-990
Closed Access | Times Cited: 41
Synthesis of 7′-Arylidenespiro[indoline-3,1′-pyrrolizines] and 7′-Arylidenespiro[indene-2,1′-pyrrolizines] via [3 + 2] Cycloaddition and β-C–H Functionalized Pyrrolidine
Ying Huang, Hui‐Lin Fang, Yixin Huang, et al.
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 19, pp. 12437-12451
Closed Access | Times Cited: 41
Synthesis, TD-DFT calculations, molecular docking and ADME studies of new spiro-oxindole derivatives containing 5(4H)-oxazolone as anti-viral and anti-bacterial agents
Nosrat Madadi Mahani, H. Hamidian, Samieh Fozooni, et al.
Journal of Computer-Aided Molecular Design (2025) Vol. 39, Iss. 1
Closed Access
An unprecedented base-promoted domino reaction of methyleneindolinones and N-tosyloxycarbamates for the construction of bispirooxindoles and spiroaziridine oxindoles
Qilin Wang, Tian Cai, Jing Zhou, et al.
Chemical Communications (2015) Vol. 51, Iss. 53, pp. 10726-10729
Closed Access | Times Cited: 37
Squaramide‐Catalyzed Enantioselective Cascade Approach to Bispirooxindoles with Multiple Stereocenters
Bo‐Liang Zhao, Da‐Ming Du
Advanced Synthesis & Catalysis (2016) Vol. 358, Iss. 24, pp. 3992-3998
Closed Access | Times Cited: 32
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
Assembly of Indolenines, 3-Amino Oxindoles, and Aldehydes into Indolenine-Substituted Spiro[pyrrolidin-2,3′-oxindoles] via 1,3-Dipolar Cycloaddition with Divergent Diastereoselectivities
Guodong Zhu, Siyuan Liu, Shiqi Wu, et al.
The Journal of Organic Chemistry (2017) Vol. 82, Iss. 8, pp. 4317-4327
Closed Access | Times Cited: 32
Highly stereoselective construction of novel dispirooxindole–imidazolidines via self-1,3-dipolar cyclization of ketimines
Yanhua Sun, Yu Xiong, Chuqin Peng, et al.
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 29, pp. 7907-7910
Closed Access | Times Cited: 28
A simple oxindole-based colorimetric HSO4¯ sensor: Naked-eye detection and spectroscopic analysis
Sinan Bayındır, Ferruh Lafzi
Journal of Photochemistry and Photobiology A Chemistry (2019) Vol. 376, pp. 146-154
Closed Access | Times Cited: 23
Synthesis of Bis-pyrrolizidine-Fused Dispiro-oxindole Analogues of Curcumin via One-Pot Azomethine Ylide Cycloaddition: Experimental and Computational Approach toward Regio- and Diastereoselection
Yogesh P. Bharitkar, Mohua Das, Neha Kumari, et al.
Organic Letters (2015) Vol. 17, Iss. 18, pp. 4440-4443
Closed Access | Times Cited: 24
Regio- and diastereoselective construction of a new set of functionalized pyrrolidine, spiropyrrolidine and spiropyrrolizidine scaffolds appended with aryl- and heteroaryl moieties via the azomethine ylide cycloadditions
Vadla Rajkumar, Srinivasarao Arulananda Babu, Rayavarapu Padmavathi
Tetrahedron (2016) Vol. 72, Iss. 36, pp. 5578-5594
Closed Access | Times Cited: 20
Base-catalyzed one-pot synthesis of dispiro-1,3-dioxolane bisoxindoles from N-methylisatin and methyl propiolate
Su Yeon Kim, Hwa Jung Roh, Da Young Seo, et al.
Tetrahedron Letters (2017) Vol. 58, Iss. 10, pp. 914-918
Closed Access | Times Cited: 19
Asymmetric Organocatalytic Assembly of Oxindoles Fused with Spiro‐3,4‐dihydropyrans with Three Contiguous Stereocenters Consisting of Vicinal Quaternary Centers
Manjunatha Vishwanath, Poopathy Vinayagam, V. Pratap Reddy Gajulapalli, et al.
Asian Journal of Organic Chemistry (2016) Vol. 5, Iss. 5, pp. 613-616
Closed Access | Times Cited: 18
Regio- and stereoselective synthesis of spiro-heterocycles bearing the pyrazole scaffold via [3+2] cycloaddition reaction
Mohammad Shahidul Islam, Matti Haukka, Saied M. Soliman, et al.
Journal of Molecular Structure (2021) Vol. 1250, pp. 131711-131711
Closed Access | Times Cited: 15
Three-component [3 + 2] cycloaddition for regio- and diastereoselective synthesis of spirooxindole-pyrrolidines
Xiaofeng Zhang, Miao Liu, Desheng Zhan, et al.
New Journal of Chemistry (2022) Vol. 46, Iss. 8, pp. 3866-3870
Open Access | Times Cited: 10
Page 1 - Next Page

Scroll to top