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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.

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Showing 1-25 of 28 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
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
Anticancer potential of spirocompounds in medicinal chemistry: A pentennial expedition
Darshana Bora, Anjali Kaushal, Nagula Shankaraiah
European Journal of Medicinal Chemistry (2021) Vol. 215, pp. 113263-113263
Closed Access | Times Cited: 79
Electrochemical Multicomponent Cascade Radical Process Enabling Synthesis of Iodomethyl Spiropyrrolidinyl‐Oxindoles
Jingrui He, Haibo Mei, Jorge Escorihuela, et al.
Chinese Journal of Chemistry (2024) Vol. 42, Iss. 15, pp. 1691-1698
Closed Access | Times Cited: 9
Pyrrolo[2,1-a]isoquinoline scaffolds for developing anti-cancer agents
Leidy J. García Maza, Arturo René Mendoza Salgado, Vladímir V. Kouznetsov, et al.
RSC Advances (2024) Vol. 14, Iss. 3, pp. 1710-1728
Open Access | Times Cited: 8
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
Stereoselective synthesis of fused-, spiro- and bridged heterocycles via cyclization of isoquinolinium salts: a recent update
Suven Das
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 9, pp. 1838-1868
Closed Access | Times Cited: 25
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
Highly diastereoselective construction of novel dispiropyrrolo[2,1-a]isoquinoline derivativesviamulticomponent 1,3-dipolar cycloaddition of cyclic diketones-based tetrahydroisoquinoliniumN-ylides
Sarra Boudriga, Saoussen Haddad, Moheddine Askri, et al.
RSC Advances (2019) Vol. 9, Iss. 20, pp. 11082-11091
Open Access | Times Cited: 32
Diastereoselective synthesis of dispiro[indoline-3,3′-furan-2′,3′′-pyrrolidine] via [3 + 2]cycloaddition reaction of MBH maleimides of isatins and 1,3-dicarbonyl compounds
Liu‐Na Pan, Jing Sun, Rong‐Guo Shi, et al.
Organic Chemistry Frontiers (2020) Vol. 7, Iss. 20, pp. 3202-3208
Closed Access | Times Cited: 29
Condensation-Based Methods for the C–H Bond Functionalization of Amines
Daniel Seidel, Weijie Chen
Synthesis (2021) Vol. 53, Iss. 21, pp. 3869-3908
Open Access | Times Cited: 25
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
Facile one-pot synthesis of spirooxindole-pyrrolidine derivatives and their antimicrobial and acetylcholinesterase inhibitory activities
Ying Huang, Min Wei, Qiu-Wen Wu, et al.
New Journal of Chemistry (2018) Vol. 42, Iss. 19, pp. 16211-16216
Closed Access | Times Cited: 27
Decade Advance of Isatin in Three‐component Reactions
Shuaijie Zhang, Dayun Huang, Jinjing Wu, et al.
Asian Journal of Organic Chemistry (2022) Vol. 12, Iss. 2
Closed Access | Times Cited: 10
1,3-Dipolar cycloaddition reactions of isatin-derived azomethine ylides for the synthesis of spirooxindole and indole-derived scaffolds: recent developments
Fatemeh Rostami Miankooshki, Mohammad Bayat, Shima Nasri, et al.
Molecular Diversity (2022) Vol. 27, Iss. 5, pp. 2365-2397
Closed Access | Times Cited: 9
One-pot synthesis, structural study, in silico and in vitro anticancer evaluation of spiropyrrolidine oxindoles obtained by the 3-CR of isatin, benzyl amine and a thiazolo[3,2-a]indole derivative
C.B. Meenakshy, Athul Sudheendranath, Noble V. Thomas, et al.
Journal of Molecular Structure (2023) Vol. 1298, pp. 137026-137026
Closed Access | Times Cited: 4
Asymmetric synthesis of isoxazole and trifluoromethyl-containing 3,2′-pyrrolidinyl dispirooxindoles via squaramide-catalysed [3 + 2] cycloaddition reactions
Tong-Hao Li, Da‐Ming Du
Organic & Biomolecular Chemistry (2021) Vol. 20, Iss. 4, pp. 817-823
Closed Access | Times Cited: 10
Stereoselective Synthesis of Dispirooxindoles Incorporating Pyrrolo[2,1-a]isoquinoline via [3+2] Cycloaddition of Azomethine Ylides with a Thiazolo[3,2-a]indole Dipolarophile
Ani Deepthi, Noble V. Thomas, C.B. Meenakshy, et al.
Synthesis (2022) Vol. 54, Iss. 12, pp. 2885-2893
Closed Access | Times Cited: 7
Selective and Reversible 1,3-Dipolar Cycloaddition of 2-(2-Oxoindoline-3-ylidene)acetates with Nitrones in the Synthesis of Functionalized Spiroisoxazolidines
Dmitriy D. Karcev, Мария М. Ефремова, A. P. Molchanov, et al.
International Journal of Molecular Sciences (2022) Vol. 23, Iss. 20, pp. 12639-12639
Open Access | Times Cited: 6
3-Phenacylideneoxindoles in organic synthesis: Recent developments
Fatemeh Doraghi, Mohammad Javad Karimi, Bahareh Bari, et al.
Tetrahedron Letters (2023) Vol. 129, pp. 154725-154725
Closed Access | Times Cited: 3
Highly stereoselective dearomative [3 + 2] cycloadditon of cyclic pyridinium ylides to access spiro-indolizidine scaffolds
Xiao‐Long He, Cheng Wang, You‐Wu Wen, et al.
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 20, pp. 5847-5851
Closed Access | Times Cited: 7
C1‐Functionalization of 1,2,3,4‐Tetrahydroisoquinolines (THIQs)
Zahra Tashrifi, Mohammad Mohammadi Khanaposhtani, Bagher Larijani, et al.
Asian Journal of Organic Chemistry (2021) Vol. 10, Iss. 10, pp. 2421-2439
Closed Access | Times Cited: 7
Synthesis of Hexahydropyrrolo-isoquinolines by 1,3-Dipolar cycloaddition of tetrahydroisoquinolines and cinnamaldehydes
You-Gui Li, Weike Chen, You-Qiang Guo, et al.
Tetrahedron Letters (2023) Vol. 122, pp. 154519-154519
Closed Access | Times Cited: 2
Domino β‐C−H Functionalization and [3+2] Cycloaddition for Efficient Synthesis of Diverse Spiro and Polycyclic Compounds
Hui‐Lin Fang, Ying Han, Jing Sun, et al.
ChemistrySelect (2020) Vol. 5, Iss. 44, pp. 14086-14090
Closed Access | Times Cited: 4
Diastereoselective Three-Component 1,3-Dipolar Cycloaddition to Access Functionalized β-Tetrahydrocarboline- and Tetrahydroisoquinoline-Fused Spirooxindoles
Yongchao Wang, Yu Chen, Shengli Duan, et al.
Molecules (2024) Vol. 29, Iss. 8, pp. 1790-1790
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