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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:

Diastereodivergent asymmetric Michael-alkylation reactions using chiralN,N′-dioxide/metal complexes
Yulong Kuang, Bin Shen, Li Dai, et al.
Chemical Science (2017) Vol. 9, Iss. 3, pp. 688-692
Open Access | Times Cited: 52

Showing 1-25 of 52 citing articles:

Catalytic asymmetric synthesis of spirooxindoles: recent developments
Guang‐Jian Mei, Feng Shi
Chemical Communications (2018) Vol. 54, Iss. 50, pp. 6607-6621
Closed Access | Times Cited: 400
Palladium-Catalyzed Diastereoselective Formal [5 + 3] Cycloaddition for the Construction of Spirooxindoles Fused with an Eight-Membered Ring
Ben Niu, Xiao‐Yun Wu, Yin Wei, et al.
Organic Letters (2019) Vol. 21, Iss. 12, pp. 4859-4863
Closed Access | Times Cited: 80
Bimetallic Ru/Ru‐Catalyzed Asymmetric One‐Pot Sequential Hydrogenations for the Stereodivergent Synthesis of Chiral Lactones
Jingli He, Zhaodi Li, Ruhui Li, et al.
Advanced Science (2024) Vol. 11, Iss. 23
Open Access | Times Cited: 8
Catalytic Asymmetric Synthesis of Chiral Spiro‐cyclopropyl Oxindoles from 3‐Alkenyl‐oxindoles and Sulfoxonium Ylides
Lifeng Wang, Weidi Cao, Hongjiang Mei, et al.
Advanced Synthesis & Catalysis (2018) Vol. 360, Iss. 21, pp. 4089-4093
Closed Access | Times Cited: 47
NHC-catalysed retro-aldol/aldol cascade reaction enabling solvent-controlled stereodivergent synthesis of spirooxindoles
Hai‐Jun Leng, Qian Zhao, Qing Mao, et al.
Chinese Chemical Letters (2021) Vol. 32, Iss. 8, pp. 2567-2571
Closed Access | Times Cited: 30
Unveiling the beauty of cyclopropane formation: a comprehensive survey of enantioselective Michael initiated ring closure (MIRC) reactions
Ramkumar Moorthy, Waidath Bio-Sawe, Sagar S. Thorat, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 16, pp. 4560-4601
Open Access | Times Cited: 4
Reversal of enantioselectivity in cobalt(ii)-catalyzed asymmetric Michael–alkylation reactions: synthesis of spiro-cyclopropane-oxindoles
Jun-Hao Zhang, Weijing Yang, Ning Li, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 14, pp. 4007-4013
Closed Access | Times Cited: 4
Highly stereo- and enantio-selective synthesis of spiro- cyclopropyl oxindoles via organic catalyst-mediated cyclopropanation
Min Liu, Di Wang, Zenghui Ye, et al.
Chinese Chemical Letters (2025), pp. 110923-110923
Closed Access
Synthesis of Spiro 3,3′-Cyclopropyl Oxindoles via Cyclopropanation of 3-Alkenyl-oxindoles with CF3-Imidoyl Sulfoxonium Ylides
Chen Li, Yu Zhang, Zhengkai Chen
The Journal of Organic Chemistry (2025)
Closed Access
Controllable synthesis of 3-chloro- and 3,3-dichloro-2-oxindoles via hypervalent iodine-mediated chlorooxidation
Xinpeng Jiang, Liechao Yang, Wenlong Yang, et al.
Organic & Biomolecular Chemistry (2019) Vol. 17, Iss. 28, pp. 6920-6924
Closed Access | Times Cited: 30
Asymmetric Catalytic Diverse Ring Opening/Cycloadditions of Cyclobutenones with (E)-Alkenyloxindoles and (E)-Dioxopyrrolidines
Yao Luo, Hang Zhang, Siyuan Wang, et al.
Organic Letters (2020) Vol. 22, Iss. 7, pp. 2645-2650
Closed Access | Times Cited: 28
Asymmetric Synthesis of Chiral Cyclopropanes from Sulfoxonium Ylides Catalyzed by a Chiral-at-Metal Rh(III) Complex
Jixin Pian, Qingqing Chen, Yujiao Luo, et al.
Organic Letters (2022) Vol. 24, Iss. 31, pp. 5641-5645
Closed Access | Times Cited: 16
Diastereodivergent synthesis of cyclopropanes via on-water [2 + 1] annulations of diazo compounds with electron-deficient alkenes
Qing‐Zhu Li, Xiang Zhang, Ke Xie, et al.
Green Chemistry (2019) Vol. 21, Iss. 9, pp. 2375-2379
Closed Access | Times Cited: 29
Asymmetric synthesis of spirooxindole-fused spirothiazolonesviasquaramide-catalysed reaction of 3-chlorooxindoles with 5-alkenyl thiazolones
Yong‐Xing Song, Da‐Ming Du
Organic & Biomolecular Chemistry (2019) Vol. 17, Iss. 21, pp. 5375-5380
Closed Access | Times Cited: 28
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
Organocatalytic asymmetric synthesis of highly functionalized spiro-thiazolone–cyclopropane-oxindoles bearing two vicinal spiro quaternary centers
Shengzheng Wang, Zhongjie Guo, Ying Wu, et al.
Organic Chemistry Frontiers (2019) Vol. 6, Iss. 9, pp. 1442-1447
Closed Access | Times Cited: 23
Divergent synthesis of oxindole derivatives via controllable reactions of isatin-derived para-quinone methides with sulfur ylides
Yong You, Bao-Xue Quan, Zhen‐Hua Wang, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 24, pp. 4560-4565
Closed Access | Times Cited: 23
Further developments of β,γ-unsaturated α-ketoesters as versatile synthons in asymmetric catalysis
Ruixian Deng, Tian‐Jiao Han, Xiang Gao, et al.
iScience (2022) Vol. 25, Iss. 3, pp. 103913-103913
Open Access | Times Cited: 13
Asymmetric Synthesis of Spiro-3,3′-cyclopropyl Oxindoles via Vinylogous Michael Initiated Ring Closure Reaction
Abhijit Manna, Harshit Joshi, Vinod K. Singh
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 24, pp. 16755-16766
Closed Access | Times Cited: 13
Organocatalytic Enantioselective Synthesis of Nitrocyclopropanes Bearing a Thioester Group and Three Stereogenic Centers
Bingfu Wang, Jian Liu, Hui Jin, et al.
Advanced Synthesis & Catalysis (2024) Vol. 366, Iss. 12, pp. 2742-2748
Closed Access | Times Cited: 2
Palladium/copper-cocatalyzed three-component tandem cyclization of o-alkenyl arylisocyanides, sulfur ylides with alcohols: direct synthesis of spiro 3,3’-cyclopropyl oxindoles
Yue Gong, Xue-Cen Xu, Zixuan Yang, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 12, pp. 3369-3375
Closed Access | Times Cited: 2
Copper‐Catalyzed Dimerization of Sulfoxonium Ylides with 3‐Diazoindolin‐2‐imines: A Practical and Efficient Approach to Spiro[cyclopropane‐1,3′‐indolin]‐2′‐imines
Muhammad Suleman, Zhenmin Li, Ping Lü, et al.
European Journal of Organic Chemistry (2019) Vol. 2019, Iss. 27, pp. 4447-4456
Closed Access | Times Cited: 20
Divergent syntheses of spirooxindoles from oxindole-embedded four-membered synthon via cycloaddition reactions
Hongjin Shi, Liang Wang, Shuai‐Shuai Li, et al.
Organic Chemistry Frontiers (2020) Vol. 7, Iss. 5, pp. 747-755
Closed Access | Times Cited: 20
Recent advances in the rare-earth metal triflates-catalyzed organic reactions
Yue‐Hua Wu, Lei-Yang Zhang, Nai‐Xing Wang, et al.
Catalysis Reviews (2020) Vol. 64, Iss. 4, pp. 679-715
Closed Access | Times Cited: 19
SO2ClF: A Reagent for Controllable Chlorination and Chlorooxidation of Simple Unprotected Indoles
Tianting Ma, Yu Zheng, Shenlin Huang
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 7, pp. 4839-4847
Closed Access | Times Cited: 6
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