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:
Cu(i )-Catalyzed asymmetric exo-selective synthesis of substituted pyrrolidines via a 1,3-dipolar cycloaddition reaction
Rayhan G. Biswas, Sumit Kumar Ray, Vinod K. Kannaujiya, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 21, pp. 4685-4690
Closed Access | Times Cited: 8
Rayhan G. Biswas, Sumit Kumar Ray, Vinod K. Kannaujiya, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 21, pp. 4685-4690
Closed Access | Times Cited: 8
Showing 8 citing articles:
Catalytic Enantioselective [3+2] Cycloaddition of N‐Metalated Azomethine Ylides
Sundaravel Vivek Kumar, Patrick J. Guiry
Chemistry - A European Journal (2023) Vol. 29, Iss. 28
Open Access | Times Cited: 28
Sundaravel Vivek Kumar, Patrick J. Guiry
Chemistry - A European Journal (2023) Vol. 29, Iss. 28
Open Access | Times Cited: 28
Electron-rich benzofulvenes as effective dipolarophiles in copper(i )-catalyzed asymmetric 1,3-dipolar cycloaddition of azomethine ylides
Xin Chang, Xue‐Tao Liu, Fangfang Li, et al.
Chemical Science (2023) Vol. 14, Iss. 20, pp. 5460-5469
Open Access | Times Cited: 11
Xin Chang, Xue‐Tao Liu, Fangfang Li, et al.
Chemical Science (2023) Vol. 14, Iss. 20, pp. 5460-5469
Open Access | Times Cited: 11
Asymmetric Catalytic Synthesis of Hexahydropyrrolo‐isoquinolines via Three‐Component 1,3‐Dipolar‐Cycloaddition
Zhaojing Li, Nian Xu, Ning Guo, et al.
Chemistry - A European Journal (2021) Vol. 27, Iss. 60, pp. 14841-14845
Closed Access | Times Cited: 14
Zhaojing Li, Nian Xu, Ning Guo, et al.
Chemistry - A European Journal (2021) Vol. 27, Iss. 60, pp. 14841-14845
Closed Access | Times Cited: 14
Asymmetric Umpolung (3+2) Cycloadditions of Iminoesters with α,β-Unsaturated-2-acyl Imidazoles for the Synthesis of Substituted Pyrrolidines
Mamta Gill, Arko Das, Vinod K. Singh
Organic Letters (2022) Vol. 24, Iss. 31, pp. 5629-5634
Closed Access | Times Cited: 9
Mamta Gill, Arko Das, Vinod K. Singh
Organic Letters (2022) Vol. 24, Iss. 31, pp. 5629-5634
Closed Access | Times Cited: 9
Asymmetric Formal (3 + 2) Cyclocondensation of Coumarin-3-Formylpyrazoles as 3-Carbon Partners with 3-Hydroxyoxindoles via Esterification/Michael Addition Sequence
Shijie Zhu, Zhi-Feng Hao, Pan Ya, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 22, pp. 15210-15223
Closed Access | Times Cited: 8
Shijie Zhu, Zhi-Feng Hao, Pan Ya, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 22, pp. 15210-15223
Closed Access | Times Cited: 8
Enantioselective synthesis of substituted 1-pyrrolines via Michael addition of iminoesters with α,β-unsaturated 2-acyl imidazoles catalyzed by chiral Cu(I)-BPE complex
Mamta Gill, Vinod K. Singh
Tetrahedron Letters (2023) Vol. 123, pp. 154555-154555
Closed Access | Times Cited: 3
Mamta Gill, Vinod K. Singh
Tetrahedron Letters (2023) Vol. 123, pp. 154555-154555
Closed Access | Times Cited: 3
An unexpected Michael type addition-deacylpyrazole involving coumarin-3-formylpyrazoles under mild conditions
Chuan-Wen Lei, J. van der Lei, Xiaoli Feng, et al.
Tetrahedron (2024) Vol. 169, pp. 134360-134360
Closed Access
Chuan-Wen Lei, J. van der Lei, Xiaoli Feng, et al.
Tetrahedron (2024) Vol. 169, pp. 134360-134360
Closed Access
Progress in Catalytic Asymmetric Reactions with 7-Azaindoline as the Directing Group
Yanping Zhang, Yong You, Jun‐Qing Yin, et al.
Molecules (2023) Vol. 28, Iss. 23, pp. 7898-7898
Open Access | Times Cited: 1
Yanping Zhang, Yong You, Jun‐Qing Yin, et al.
Molecules (2023) Vol. 28, Iss. 23, pp. 7898-7898
Open Access | Times Cited: 1
