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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:

Hydroxyl-group-activated azomethine ylides in organocatalytic H-bond-assisted 1,3-dipolar cycloadditions and beyond
Artur Przydacz, Jan Bojanowski, Anna Albrecht, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 14, pp. 3075-3086
Closed Access | Times Cited: 22

Showing 22 citing articles:

Catalytic Asymmetric Dearomative 1,3-Dipolar Cycloaddition of 2-Nitrobenzothiophenes and Isatin-Derived Azomethine Ylides
Jian‐Qiang Zhao, Zhou Shun, Lei Yang, et al.
Organic Letters (2021) Vol. 23, Iss. 21, pp. 8600-8605
Closed Access | Times Cited: 41

Intramolecular Hydrogen-Bond Activation: Strategies, Benefits, and Influence in Catalysis
Andrea Guerrero‐Corella, Alberto Fraile, José Alemán
ACS Organic & Inorganic Au (2022) Vol. 2, Iss. 3, pp. 197-204
Open Access | Times Cited: 26

Construction of heterocyclic rings from cyclopropenes
Hengrui Huo, Yuefa Gong
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 19, pp. 3847-3869
Closed Access | Times Cited: 22

Brønsted base-catalyzed assembly of sulfochromeno[4,3-b]pyrrolidines via tandem [3 + 2] cycloaddition–SuFEx click reaction of ethenesulfonyl fluorides and o-hydroxyaryl azomethines
Fang Zhang, Qichao Zhang, Pei Xie, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 21, pp. 6177-6183
Closed Access | Times Cited: 3

Organocatalysis in 1,3-Dipolar Cycloaddition Reactions (A Review)
Yulia A. Pronina, L. A. Teglyai, A. I. Ponyaev, et al.
Russian Journal of General Chemistry (2024) Vol. 94, Iss. 1, pp. 1-44
Closed Access | Times Cited: 2

Copper-catalyzed asymmetric propargylic substitution with salicylaldehyde-derived imine esters
Ruo‐Qing Wang, Chong Shen, Xiang Cheng, et al.
Chemical Communications (2022) Vol. 58, Iss. 61, pp. 8552-8555
Closed Access | Times Cited: 10

Highly Chemoselective Synthesis of Purino[3,2-c]oxazoles via the Asymmetric Dearomative [3+2] Cycloaddition of Purines with Donor–Acceptor Oxiranes
Meng‐Cheng Zhang, Dong‐Chao Wang, Hai‐Ting Wang, et al.
Organic Letters (2022) Vol. 24, Iss. 41, pp. 7527-7532
Closed Access | Times Cited: 9

Synthesis of pyrrolidin-2-ylidenes and pyrrol-2-ylidenes via 1,3-dipolar cycloaddition of H-bond-assisted azomethine ylides to nitrostyrenes
Issa Yavari, Ramin Mohsenzadeh, Parisa Ravaghi, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 25, pp. 5265-5273
Closed Access | Times Cited: 5

Asymmetric synthesis of aryl‐substituted pyrrolidines by using CFAM ligand–AgOAc chiral system via 1,3‐dipolar cycloaddition reaction
Nurzhan Beksultanova, Özdemir Doğan
Chirality (2023) Vol. 35, Iss. 7, pp. 435-448
Closed Access | Times Cited: 4

Divergent synthesis of pyrrolidine and glutamic acid derivatives using a macrocyclic phase-transfer catalyst under high-pressure conditions
Agata Tyszka‐Gumkowska, Janusz Jurczak
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 20, pp. 5888-5894
Closed Access | Times Cited: 10

Perfluoroalkyl-Promoted Synthesis of Perfluoroalkylated Pyrrolidine-Fused Coumarins with Methyl β-Perfluoroalkylpropionates
Nan Qi Ren, Lingfeng Zhang, Yijie Hu, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 21, pp. 15717-15725
Closed Access | Times Cited: 9

Diastereodivergent 1,3‐Dipolar Cycloaddition of α‐Fluoro‐α,β‐Unsaturated Arylketones and Azomethine Ylides: Experimental and Theoretical DFT Studies
Subarna Jyoti Kalita, Zhen‐Ni Zhao, Zi‐Han Li, et al.
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 40, pp. 5530-5535
Closed Access | Times Cited: 7

Synthesis of Hexahydropyrrolo-isoquinolines by 1,3-Dipolar cycloaddition of tetrahydroisoquinolines and cinnamaldehydes
You-Gui Li, Weike Chen, You-Qiang Guo, et al.
Tetrahedron Letters (2023) Vol. 122, pp. 154519-154519
Closed Access | Times Cited: 2

Alkylidene Meldrum′s Acid as Acceptor‐Donor‐Acceptor with Azomethine Ylide for Organocatalytic Asymmetric (3+2) Cycloaddition/Annulation: Synthesis of Chromeno[4,3‐b]pyrrolidine
Yan‐Cheng Liou, Yi‐Ru Chen, Ching‐Wen Hsu, et al.
Advanced Synthesis & Catalysis (2023) Vol. 365, Iss. 21, pp. 3603-3610
Closed Access | Times Cited: 2

Dearomative, aminocatalytic formal normal-electron-demand aza-Diels–Alder cycloaddition in the synthesis of tetrahydrofuropyridines
Mateusz Dyguda, Artur Przydacz, Łukasz Albrecht
Chemical Communications (2023) Vol. 59, Iss. 86, pp. 12903-12906
Closed Access | Times Cited: 2

Enantioselective, Decarboxylative (3+2)-Cycloaddition of Azomethine Ylides and Chromone-3-Carboxylic Acids
Ewelina Kowalska, Lesław Sieroń, Anna Albrecht
Molecules (2022) Vol. 27, Iss. 20, pp. 6809-6809
Open Access | Times Cited: 1

Reactions of Arylaldimines of Glycine Ethyl Ester with Halo-Substituted Arylideneacetones
S. G. Kostryukov, V. A. Kalyazin, P. S. Petrov, et al.
Russian Journal of General Chemistry (2023) Vol. 93, Iss. 6, pp. 1311-1321
Closed Access

Synthesis of Spiro[pyrrole-3,2'-pyrrolo[2,1-b]oxazoles] via 1,3-Dipolar Cycloaddition of 1H-Pyrrole-2,3-diones to Azomethine Ylides
A. A. Moroz, М. V. Dmitriev, А. Н. Масливец
Russian Journal of Organic Chemistry (2023) Vol. 59, Iss. 11, pp. 1867-1873
Closed Access

Reactions of arylaldimines of glycine ethyl ester with halo-substituted arylideneacetones
S. G. Kostryukov, V. A. Kalyazin, P. S. Petrov, et al.
Журнал Общей Химии (2023) Vol. 93, Iss. 6, pp. 823-834
Closed Access

Synthesis of spiro[pyrrole-3,2'-pyrrolo[2,1-<i>b</i>]oxazoles] via 1,3-dipolar cycloaddition of 1<i>H</i>-pyrrole-2,3-diones to azomethine ylides
A. A. Moroz, М. V. Dmitriev, А. Н. Масливец
Журнал органической химии (2023) Vol. 59, Iss. 11, pp. 1427-1434
Closed Access

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