OpenAlex Citation Counts

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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:

Diastereo- and enantioselective [3 + 3] cycloaddition of spirocyclopropyl oxindoles using both aldonitrones and ketonitrones
Pengwei Xu, Jia-Kuan Liu, Lan Shen, et al.
Nature Communications (2017) Vol. 8, Iss. 1
Open Access | Times Cited: 98

Showing 1-25 of 98 citing articles:

Catalytic Enantioselective Ring-Opening Reactions of Cyclopropanes
Vincent Pirenne, Bastian Muriel, Jérôme Waser
Chemical Reviews (2020) Vol. 121, Iss. 1, pp. 227-263
Open Access | Times Cited: 408

Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles
Zhong‐Yan Cao, Feng Zhou, Jian Zhou
Accounts of Chemical Research (2018) Vol. 51, Iss. 6, pp. 1443-1454
Closed Access | Times Cited: 373

Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters
Pengwei Xu, Jin‐Sheng Yu, Chen Chen, et al.
ACS Catalysis (2019) Vol. 9, Iss. 3, pp. 1820-1882
Closed Access | Times Cited: 273

Asymmetric Catalytic Reactions of Donor–Acceptor Cyclopropanes
Yong Xia, Xiaohua Liu, Xiaoming Feng
Angewandte Chemie International Edition (2020) Vol. 60, Iss. 17, pp. 9192-9204
Closed Access | Times Cited: 170

Regio‐ and Enantioselective (3+3) Cycloaddition of Nitrones with 2‐Indolylmethanols Enabled by Cooperative Organocatalysis
Tian‐Zhen Li, Si‐Jia Liu, Yu‐Wen Sun, et al.
Angewandte Chemie International Edition (2020) Vol. 60, Iss. 5, pp. 2355-2363
Closed Access | Times Cited: 104

Catalytic selective mono- and difluoroalkylation using fluorinated silyl enol ethers
Xiao‐Si Hu, Jin‐Sheng Yu, Jian Zhou
Chemical Communications (2019) Vol. 55, Iss. 91, pp. 13638-13648
Closed Access | Times Cited: 97

2-Oxindole and related heterocycles: synthetic methodologies for their natural products and related derivatives
Shivangi Sharma, Yukti Monga, Ashu Gupta, et al.
RSC Advances (2023) Vol. 13, Iss. 21, pp. 14249-14267
Open Access | Times Cited: 33

Hydride Transfer Involved Redox-Neutral Cascade Cyclizations for Construction of Spirocyclic Bisoxindoles Featuring a [3,4]-Fused Oxindole Moiety
Shuai‐Shuai Li, Shuai Zhu, Chunqi Chen, et al.
Organic Letters (2019) Vol. 21, Iss. 4, pp. 1058-1062
Closed Access | Times Cited: 74

Syntheses and Applications of Spirocyclopropyl Oxindoles: A Decade Review
Akash P. Sakla, Pritish Kansal, Nagula Shankaraiah
European Journal of Organic Chemistry (2020) Vol. 2021, Iss. 5, pp. 757-772
Closed Access | Times Cited: 64

1,3-Dipolar cycloaddition of nitrones: synthesis of multisubstituted, diverse range of heterocyclic compounds
S. B. THAKUR, Arunima Das, Tapas Das
New Journal of Chemistry (2021) Vol. 45, Iss. 26, pp. 11420-11456
Closed Access | Times Cited: 49

Catalytic (3 + 2) annulation of donor–acceptor aminocyclopropane monoesters and indoles
Vincent Pirenne, Emma G. L. Robert, Jérôme Waser
Chemical Science (2021) Vol. 12, Iss. 25, pp. 8706-8712
Open Access | Times Cited: 45

Thiourea participation in [3+2] cycloaddition with donor–acceptor cyclopropanes: a domino process to 2-amino-dihydrothiophenes
Ming‐Sheng Xie, Guofeng Zhao, Tao Qin, et al.
Chemical Communications (2019) Vol. 55, Iss. 11, pp. 1580-1583
Closed Access | Times Cited: 53

Stereocontrolled Synthesis of Bispirooxindole-Based Hexahydroxanthones with Five Contiguous Stereocenters
Xiong‐Li Liu, Gen Zhou, Yi Gong, et al.
Organic Letters (2019) Vol. 21, Iss. 8, pp. 2528-2531
Closed Access | Times Cited: 52

Bifunctional oxindole-chromone 4C building block directed asymmetric synthesis of bispirocyclic hexahydroxanthones featuring five contiguous stereocenters and two side-by-side oxindoles
Xiong‐Li Liu, Yi Gong, Shuang Chen, et al.
Organic Chemistry Frontiers (2019) Vol. 6, Iss. 10, pp. 1603-1607
Closed Access | Times Cited: 52

Domino Corey–Chaykovsky Reaction for One-Pot Access to Spirocyclopropyl Oxindoles
Saumen Hajra, Sayan Roy, SK Abu Saleh
Organic Letters (2018) Vol. 20, Iss. 15, pp. 4540-4544
Closed Access | Times Cited: 49

One-Pot Au[III]-/Lewis Acid Catalyzed Cycloisomerization of Nitroalkynes and [3 + 3]Cycloaddition with Donor–Acceptor Cyclopropanes
Pawan S. Dhote, Chepuri V. Ramana
Organic Letters (2019) Vol. 21, Iss. 16, pp. 6221-6224
Closed Access | Times Cited: 48

Recent Advances in Stereoselective Ring Expansion of Spirocyclopropanes: Access to the Spirocyclic Compounds
Tanumay Sarkar, Bijay Ketan Das, Kangkan Talukdar, et al.
ACS Omega (2020) Vol. 5, Iss. 41, pp. 26316-26328
Open Access | Times Cited: 42

Enantioselective (8+3) Cycloadditions by Activation of Donor–Acceptor Cyclopropanes Employing Chiral Brønsted Base Catalysis
David McLeod, Mathias Kirk Thøgersen, Casper L. Barløse, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 29
Open Access | Times Cited: 26

Formal oxygen atom insertion as a skeletal-editing step: rapid access natural-product-inspired bispiro[oxindole-oxazinane] hybrids
Qing-Hui Shi, Yu‐Heng Wang, Zi‐Yue Chen, et al.
Organic Chemistry Frontiers (2023) Vol. 10, Iss. 13, pp. 3307-3312
Closed Access | Times Cited: 15

Synthesis of Heterocycles from Donor-Acceptor Cyclopropanes: A Five-Year Recap
Ani Deepthi, C.B. Meenakshy, Maneesh Mohan
Synthesis (2023) Vol. 55, Iss. 23, pp. 3875-3894
Closed Access | Times Cited: 14

Organocatalytic Michael/Michael Cycloaddition Enabled Asymmetric Construction of Hexahydroxanthones with Skeletal Diversity
Xiong‐Li Liu, Qi‐Di Wei, Xiong Zuo, et al.
Advanced Synthesis & Catalysis (2019) Vol. 361, Iss. 12, pp. 2836-2843
Closed Access | Times Cited: 39

Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles
Yu‐Hui Wang, Junsong Tian, Pengwei Tan, et al.
Angewandte Chemie International Edition (2019) Vol. 59, Iss. 4, pp. 1634-1643
Closed Access | Times Cited: 39

Asymmetric Catalytic Reactions of Donor–Acceptor Cyclopropanes
Yong Xia, Xiaohua Liu, Xiaoming Feng
Angewandte Chemie (2020) Vol. 133, Iss. 17, pp. 9276-9288
Closed Access | Times Cited: 33

Ring-Opening 1,3-Sulfonylation-Fluorination of Donor–Acceptor Cyclopropanes: Three-Component Access to γ-Fluorosulfones
Gwyndaf A. Oliver, Daniel B. Werz
Organic Letters (2023) Vol. 25, Iss. 19, pp. 3568-3572
Closed Access | Times Cited: 11

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