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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:

Iron(III)‐Catalyzed Arylation of Spiro‐Epoxyoxindoles with Phenols/Naphthols towards the Synthesis of Spirocyclic Oxindoles
Mupeng Luo, Rongju Yuan, Xuesong Liu, et al.
Chemistry - A European Journal (2016) Vol. 22, Iss. 28, pp. 9797-9803
Closed Access | Times Cited: 36

Showing 1-25 of 36 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
Efficient Catalytic Kinetic Resolution of Spiro‐epoxyoxindoles with Concomitant Asymmetric Friedel–Crafts Alkylation of Indoles
Gongming Zhu, Guangjun Bao, Yiping Li, et al.
Angewandte Chemie International Edition (2017) Vol. 56, Iss. 19, pp. 5332-5335
Closed Access | Times Cited: 77
FeCl3-Catalyzed synthesis of pyrrolo[1,2-a]quinoxaline derivatives from 1-(2-aminophenyl)pyrroles through annulation and cleavage of cyclic ethers
Zhenyu An, Lian‐Biao Zhao, Mingzhong Wu, et al.
Chemical Communications (2017) Vol. 53, Iss. 84, pp. 11572-11575
Closed Access | Times Cited: 70
Regioselective Ring-Opening of Spiro-Epoxyoxindoles by a Dual-Ligand Zinc-Based Metal–Organic Framework as an Efficient Heterogeneous Catalyst
Parth Patel, Unnati Patel, Bhavesh Parmar, et al.
ACS Applied Nano Materials (2022) Vol. 5, Iss. 3, pp. 3712-3721
Closed Access | Times Cited: 36
Cycloaddition Reaction of Spiro-Epoxy Oxindole with CO2 at Atmospheric Pressure Using Deep Eutectic Solvent
Raj Kumar Tak, Parth Patel, S. Saravanan, et al.
ACS Sustainable Chemistry & Engineering (2018) Vol. 6, Iss. 9, pp. 11200-11205
Closed Access | Times Cited: 51
Catalytic Kinetic Resolution of Spiro-Epoxyoxindoles with 1-Naphthols: Switchable Asymmetric Tandem Dearomatization/Oxa-Michael Reaction and Friedel–Crafts Alkylation of 1-Naphthols at the C4 Position
Gongming Zhu, Yiping Li, Guangjun Bao, et al.
ACS Catalysis (2018) Vol. 8, Iss. 3, pp. 1810-1816
Closed Access | Times Cited: 48
Enzymatic Kinetic Resolution of Bulky Spiro-Epoxyoxindoles via Halohydrin Dehalogenase-Catalyzed Enantio- and Regioselective Azidolysis
Fang-Rui Zhang, Nan‐Wei Wan, Jin-Mei Ma, et al.
ACS Catalysis (2021) Vol. 11, Iss. 15, pp. 9066-9072
Closed Access | Times Cited: 37
Gold‐Photoredox‐Cocatalyzed Tandem Oxycyclization/Coupling Sequence of Allenols and Diazonium Salts with Visible Light Mediation
Benito Alcaide, Pedro Almendros, B. Aparicio, et al.
Advanced Synthesis & Catalysis (2017) Vol. 359, Iss. 16, pp. 2789-2800
Closed Access | Times Cited: 40
An unexpected cascade reaction of 3-hydroxyoxindoles with coumarin-3-carboxylates to construct 2,3-dihydrobenzofuran spirooxindoles
Kuan Zhang, Huabin Han, Lele Wang, et al.
Chemical Communications (2019) Vol. 55, Iss. 91, pp. 13681-13684
Closed Access | Times Cited: 37
Syntheses and reactivity of spiro-epoxy/aziridine oxindole cores: developments in the past decade
Akash P. Sakla, Pritish Kansal, Nagula Shankaraiah
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 42, pp. 8572-8596
Closed Access | Times Cited: 36
Ring-Opening Cyclization (ROC) of spiro-Epoxyoxindoles with Indoles/Aldehydes: An Easy Access to Polyheterocyclic spiro-Oxindoles
Bharat Singh, Suraj Kashyap, Hitesh K. Soni, et al.
The Journal of Organic Chemistry (2025)
Closed Access
Recent Advances in the Mitsunobu and Related Reactions: A Review from 2010 to 2024
Abdeslem Bouzina, Zineb Aouf, Aïcha Amira, et al.
Topics in Current Chemistry (2025) Vol. 383, Iss. 2
Closed Access
An Unexpected [3 + 2]-Cycloaddition between Spiro-Epoxyoxindoles and γ-Deconjugated Butenolides Catalyzed by Sc(OTf)3
Jing-Liang Yu, Qian-Mao Zhang, Cheng Guo, et al.
The Journal of Organic Chemistry (2025)
Closed Access
Diastereoselective Synthesis of Dihydrobenzofuran Spirooxindoles and Their Transformation into Benzofuroquinolinones by Ring Expansion of Oxindole Core
Feng Wang, Jiaqi Pan, Ruo-Xian Shi, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 7, pp. 5142-5147
Closed Access | Times Cited: 3
Reversal of Selectivity in C3-Allylation and Formal [3 + 2]-Cycloaddition of Spiro-epoxyoxindole: Unified Synthesis of Spiro-furanooxindole, (±)-N-Methylcoerulescine, (±)-Physovenine, and 3a-Allylhexahydropyrrolo[2,3-b]indole
Saumen Hajra, Sayan Roy, Subrata Maity
Organic Letters (2017) Vol. 19, Iss. 8, pp. 1998-2001
Closed Access | Times Cited: 32
Visible-light-induced aerobic epoxidation in cyclic ether: Synthesis of spiroepoxyoxindole derivatives
Kaixiu Luo, Xianglin Yu, Peng Chen, et al.
Tetrahedron Letters (2020) Vol. 61, Iss. 10, pp. 151578-151578
Closed Access | Times Cited: 21
Regio- and stereoselective ring-opening reaction of spiro-epoxyoxindoles with ammonia under catalyst-free conditions
Bangzhi Zhang, Yiping Li, Guangjun Bao, et al.
Green Chemistry (2017) Vol. 19, Iss. 9, pp. 2107-2110
Closed Access | Times Cited: 24
FeCl3-Promoted Annulation of 2-Haloindoles: Switchable Synthesis of Spirooxindole-chromeno[2,3-b]indoles and Spirooxindole-chromeno[3,2-b]indoles
Mupeng Luo, Xinlei Zhu, Rufeng Liu, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 5, pp. 3638-3654
Closed Access | Times Cited: 18
Efficient Catalytic Kinetic Resolution of Spiro‐epoxyoxindoles with Concomitant Asymmetric Friedel–Crafts Alkylation of Indoles
Gongming Zhu, Guangjun Bao, Yiping Li, et al.
Angewandte Chemie (2017) Vol. 129, Iss. 19, pp. 5416-5419
Closed Access | Times Cited: 20
Epoxides: methods of synthesis, reactivity, practical significance
Vera L. Mamedova, Гульназ З. Хикматова, Dmitry E. Korshin, et al.
Russian Chemical Reviews (2022) Vol. 91, Iss. 11, pp. RCR5049-RCR5049
Closed Access | Times Cited: 10
Unified Approach to Fused and Spirocyclic Oxindoles through Lewis‐Acid‐Promoted Opening of Spiroepoxyoxindoles with Allylsilanes: Application to the Formal Synthesis of (±)‐Physovenine
Brijesh M. Sharma, Mahesh Yadav, Rajesh G. Gonnade, et al.
European Journal of Organic Chemistry (2017) Vol. 2017, Iss. 18, pp. 2603-2609
Closed Access | Times Cited: 14
Regioselective Alcoholysis and Hydrochlorination Reactions of Spiro‐Epoxy Oxindoles at the Spiro‐Centre: Synthesis of 3,3‐Disubstituted Oxindoles and Application for Anticancer Agents
Raj Kumar Tak, Naveen Gupta, Manish Kumar, et al.
European Journal of Organic Chemistry (2018) Vol. 2018, Iss. 41, pp. 5678-5687
Open Access | Times Cited: 14
Co(III)salen Catalyzed Enantioselective C3‐Indolylation of Spiro‐Epoxyoxindoles and Its Mechanistic Studies
Saumen Hajra, Sayan Roy, Ananda Shankar Mondal
Advanced Synthesis & Catalysis (2020) Vol. 362, Iss. 23, pp. 5475-5484
Closed Access | Times Cited: 12
Synthesis of CF3-containing spiro-epoxyoxindoles via the Corey–Chaykovsky reaction of N-alkyl isatins with Ph2S+CH2CF3OTf−
Bin Cheng, Bing Zu, Yuntong Li, et al.
Organic & Biomolecular Chemistry (2018) Vol. 16, Iss. 19, pp. 3564-3567
Closed Access | Times Cited: 12
Scandium triflate-catalyzed selective ring opening and rearrangement reaction of spiro-epoxyoxindole and carbonyl compounds
Hui Jiang, Haohua Jie, Jian Li
RSC Advances (2016) Vol. 6, Iss. 102, pp. 100307-100311
Closed Access | Times Cited: 10
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