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:

Construction of 3-amino-2-oxindoles by direct amination of aniline or α-amino-acid derivatives to 3-bromooxindoles
Min Zhao, Nai‐Kai Li, Yafei Zhang, et al.
Tetrahedron (2016) Vol. 72, Iss. 10, pp. 1406-1414
Closed Access | Times Cited: 13

Showing 13 citing articles:

Metal-Catalyzed Enantioconvergent Transformations
Miguel Yus, Carmén Nájera, Francisco Foubelo, et al.
Chemical Reviews (2023) Vol. 123, Iss. 20, pp. 11817-11893
Open Access | Times Cited: 37

Asymmetric synthesis of chiral oxindoles using isatin as starting material
Ghodsi Mohammadi Ziarani, Razieh Moradi, Negar Lashgari
Tetrahedron (2018) Vol. 74, Iss. 13, pp. 1323-1353
Closed Access | Times Cited: 65

Ionic Liquid-Mediated Hydrofluorination of o-Azaxylylenes Derived from 3-Bromooxindoles
Satoshi Mizuta, Hiroki Otaki, Ayako Kitagawa, et al.
Organic Letters (2017) Vol. 19, Iss. 10, pp. 2572-2575
Closed Access | Times Cited: 29

Thermal-mediated catalyst-free heterolytic cleavage of 3-halooxindoles: rapid access to 3-functionalized-2-oxindoles
Xiong‐Li Liu, Jing Yue, Shuang Chen, et al.
Organic Chemistry Frontiers (2018) Vol. 6, Iss. 2, pp. 256-262
Closed Access | Times Cited: 24

Enantioselective Synthesis of 3‐Substituted 3‐Amino‐2‐oxindoles by Amination with Anilines
Yang Wen-kun, Pei Dong, Jian Xu, et al.
Chemistry - A European Journal (2021) Vol. 27, Iss. 36, pp. 9272-9275
Closed Access | Times Cited: 20

Ring expansion and ring opening of 3-halooxindoles with N-alkoxycarbonyl-O-tosylhydroxylamines for divergent access to 4-aminoquinolin-2-ones and N-Cbz-N’-arylureas
Wei‐Cheng Yuan, Jian Zuo, Shu‐Pei Yuan, et al.
Organic Chemistry Frontiers (2020) Vol. 8, Iss. 4, pp. 784-791
Closed Access | Times Cited: 17

Asymmetric Synthesis of 3-Lactone-Substituted 2-Oxindoles with Vicinal Quaternary Carbon Centers through Vinylogous Conjugate Addition
Xiaohua Liu, Xiaoming Feng, Zegong Li, et al.
Synlett (2023) Vol. 34, Iss. 20, pp. 2405-2410
Closed Access | Times Cited: 6

Catalytic Enantioselective Alkylation of Aldehydes with 3-Bromooxindoles
Zhen Li, Xiao‐Ming Zhang, Fu‐Min Zhang, et al.
Organic Letters (2023) Vol. 25, Iss. 39, pp. 7252-7257
Closed Access | Times Cited: 3

Alcohols as Substrates and Solvents for the Construction of 3-Alkoxylated-2-Oxindoles by Direct Alkoxylation of 3-Halooxindoles
Bing Lin, Zhiyong Chen, Huanhuan Liu, et al.
Molecules (2017) Vol. 22, Iss. 5, pp. 801-801
Open Access | Times Cited: 6

A highly efficient method to access unprotected C-3 bifunctional quaternary 3-allyl-3-(amino)oxindoles
Xunbo Lu, Guoling Huang, Fangpeng Liang, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 17, pp. 3547-3551
Closed Access

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