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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:

Synthesis of heterocycle appended spiro(oxindole-3,2’-pyrrolidine) derivatives from heterocyclic ylidenes and azomethine ylide through 1,3-dipolar cycloaddition reactions
S. Vidya, K. Krishna Priya, Devi Velayudhan Jayasree, et al.
Synthetic Communications (2019) Vol. 49, Iss. 12, pp. 1592-1602
Closed Access | Times Cited: 20

Showing 20 citing articles:

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
Recent Strategies in the Synthesis of Spiroindole and Spirooxindole Scaffolds
Shima Nasri, Mohammad Bayat, Faezeh Mirzaei
Topics in Current Chemistry (2021) Vol. 379, Iss. 4
Closed Access | Times Cited: 61
A review on recent progress in synthesis and biological activities of spiropyrrolidine and its derivatives
A. F. M. Motiur Rahman, Md. Zafer Alam, A.H.M.M. Jahan, et al.
Journal of Molecular Structure (2025), pp. 141377-141377
Closed Access | Times Cited: 1
Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, et al.
The Chemical Record (2021) Vol. 21, Iss. 4, pp. 924-1037
Open Access | Times Cited: 43
Unveiling the high regioselectivity and stereoselectivity within the synthesis of spirooxindolenitropyrrolidine: A molecular electron density theory perspective
Nivedita Acharjee, Haydar Mohammad-Salim, Mrinmoy Chakraborty, et al.
Journal of Physical Organic Chemistry (2021) Vol. 34, Iss. 6
Closed Access | Times Cited: 31
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
Substrate‐Controlled Regioselectivity Switch in a Three‐Component 1,3‐Dipolar Cycloaddition Reaction to Access 3,3′‐Pyrrolidinyl‐Spirooxindoles Derivatives
Kai‐Kai Wang, Yan‐Li Li, Rongxiang Chen, et al.
Advanced Synthesis & Catalysis (2022) Vol. 364, Iss. 12, pp. 2047-2052
Closed Access | Times Cited: 15
Substrate-Controlled Regioselectivity Switchable [3 + 2] Annulations To Access Spirooxindole Skeletons
Kai‐Kai Wang, Yanli Li, Rongxiang Chen, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 12, pp. 8158-8169
Closed Access | Times Cited: 14
Synthesis of tryptanthrin appended dispiropyrrolidine oxindoles and their antibacterial evaluation
Sruthi Sudheendran Leena, Abdul Akhir, Deepanshi Saxena, et al.
RSC Medicinal Chemistry (2023) Vol. 14, Iss. 6, pp. 1165-1171
Closed Access | Times Cited: 8
Green Protocols for the Synthesis of 3,3’-spirooxindoles – 2016- mid 2019
Ani Deepthi, Noble V. Thomas, Vidya Sathi
Current Green Chemistry (2019) Vol. 6, Iss. 3, pp. 210-225
Closed Access | Times Cited: 23
Stereoselective Synthesis of Highly Functionalized Aminobenzothiazole-Fused Spirooxindole Derivatives: in silico and in vitro Anti-Diabetic Studies
Sivan Velmathi, Narayanasamy Nivetha, Shashank M. Patil, et al.
Synthesis (2023) Vol. 55, Iss. 24, pp. 4145-4162
Closed Access | Times Cited: 5
Stereoselective synthesis of dispiro heterocycles by [3 + 2] cycloaddition of azomethine ylides with a thiazolo[3,2-a]indole derivative
Vidya Sathi, Noble V. Thomas, Ani Deepthi
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 39, pp. 7822-7826
Closed Access | Times Cited: 14
Green Stereoselective Synthesis and In Silico Anticancer Evaluation of Tetrahydro-β-carboline-Derived Spiro Heterocycles
Ani Deepthi, Maneesh Mohan, Susan P. Eldhose, et al.
Synthesis (2023) Vol. 55, Iss. 16, pp. 2526-2536
Closed Access | Times Cited: 3
Engaging thieno[2,3‐b]indole‐2,3‐dione for the efficient synthesis of spiro[indoline‐3,4′‐thiopyrano[2,3‐b]indole] by reaction with N‐substituted isatilidenes
Noble V. Thomas, Vidya Sathi, Ani Deepthi, et al.
Journal of Heterocyclic Chemistry (2020) Vol. 58, Iss. 1, pp. 48-55
Closed Access | Times Cited: 8
Regioselective synthesis of spirooxindole-pyrolidine via (GAP) chemistry process: Experimental and DFT study
Faezeh Mataji, Leila Youseftabar‐Miri, Marjan Jebeli Javan, et al.
Journal of Molecular Structure (2022) Vol. 1270, pp. 133891-133891
Closed Access | Times Cited: 5
Multicomponent Synthesis of Heterocycles
Carolina S. Marques, Elisabete P. Carreiro, António P. S. Teixeira
Heterocycles (2022), pp. 215-275
Closed Access | Times Cited: 3
Anticancer properties of spirooxindole derivatives
Mukesh Kumar Kumawat, Narender Yadav, Kapil Kumar
Elsevier eBooks (2024), pp. 333-367
Closed Access
Interconversions of 1,3-dipolar cycloaddition products of azomethine ylides and ylidenemalononitriles
С. В. Борисова, A. A. Meshcheryakova, V. V. Sorokin
Журнал Общей Химии (2024) Vol. 94, Iss. 4, pp. 489-502
Closed Access
Recent update on the role of N-methyl glycine as a building block for the construction of N-heterocyclic frameworks
Madhu Ganesh
Tetrahedron (2022) Vol. 127, pp. 133096-133096
Closed Access | Times Cited: 2
Highly Diastereoselective Self-1,3-Dipolar [3+3] Cycloaddition of Azomethine Ylides Promoted by Cesium Catalyst
Hai Ren, Jun‐Rong Song, Xiong-Jiang Li, et al.
Heterocycles (2023) Vol. 106, Iss. 10, pp. 1687-1687
Open Access
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