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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:

Polarity effects in 4-fluoro- and 4-(trifluoromethyl)prolines
Vladimir Kubyshkin
Beilstein Journal of Organic Chemistry (2020) Vol. 16, pp. 1837-1852
Open Access | Times Cited: 17

Showing 17 citing articles:

Fluorinated Rings: Conformation and Application
Rajarshi Mondal, Mohamed Agbaria, Zackaria Nairoukh
Chemistry - A European Journal (2021) Vol. 27, Iss. 25, pp. 7193-7213
Closed Access | Times Cited: 66
Proline Analogues
Vladimir Kubyshkin, Marina Rubini
Chemical Reviews (2024) Vol. 124, Iss. 13, pp. 8130-8232
Closed Access | Times Cited: 10
Biochemistry of fluoroprolines: the prospect of making fluorine a bioelement
Vladimir Kubyshkin, Rebecca L. Davis, Nediljko Budiša
Beilstein Journal of Organic Chemistry (2021) Vol. 17, pp. 439-460
Open Access | Times Cited: 30
Fluorine-Containing Prolines: Synthetic Strategies, Applications, and Opportunities
Pavel K. Mykhailiuk
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 11, pp. 6961-7005
Closed Access | Times Cited: 22
Origami with small molecules: exploiting the C–F bond as a conformational tool
Patrick Ryan, Ramsha Iftikhar, Luke Hunter
Beilstein Journal of Organic Chemistry (2025) Vol. 21, pp. 680-716
Open Access
Copper-catalyzed [3 + 2]-cycloaddition of α-halonitroalkenes with azomethine ylides: facile synthesis of multisubstituted pyrrolidines and pyrroles
Vladimir Motornov, Andrey A. Tabolin, Yulia V. Nelyubina, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 15, pp. 3413-3427
Closed Access | Times Cited: 23
Skipped Fluorination Motifs: Synthesis of Building Blocks and Comparison of Lipophilicity Trends with Vicinal and Isolated Fluorination Motifs
Robert I. Troup, Benjamin Jeffries, Raphael El-Bekri Saudain, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 2, pp. 1882-1900
Open Access | Times Cited: 22
Experimental lipophilicity scale for coded and noncoded amino acid residues
Vladimir Kubyshkin
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 32, pp. 7031-7040
Closed Access | Times Cited: 21
Relating Conformational Equilibria to Conformer‐Specific Lipophilicities: New Opportunities in Drug Discovery
Bruno Linclau, Zhong Wang, Benjamin Jeffries, et al.
Angewandte Chemie International Edition (2021) Vol. 61, Iss. 7
Open Access | Times Cited: 19
4-Trifluoromethoxy proline: synthesis of stereoisomers and lipophilicity study
Ivan G. Logvinenko, Iryna V. Sadkova, Nataliya A. Tolmachova, et al.
Organic & Biomolecular Chemistry (2024) Vol. 22, Iss. 39, pp. 7982-7988
Closed Access | Times Cited: 1
Proline Analogues in Drug Design: Current Trends and Future Prospects
Vladimir Kubyshkin, Pavel K. Mykhailiuk
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 22, pp. 20022-20055
Closed Access | Times Cited: 1
Solvent- and functional-group-assisted tautomerism of 3-alkyl substituted 5-(2-pyridyl)-1,2,4-triazoles in DMSO–water
Jesús García López, Dmytro M. Khomenko, Borys V. Zakharchenko, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 47, pp. 9443-9458
Closed Access | Times Cited: 3
Remarkably high solvatochromism in the circular dichroism spectra of the polyproline-II conformation: limitations or new opportunities?
Vladimir Kubyshkin, Jochen Bürck, Oleg Babii, et al.
Physical Chemistry Chemical Physics (2021) Vol. 23, Iss. 47, pp. 26931-26939
Closed Access | Times Cited: 5
Physical Properties of Fluorinated Compounds
Bruno Linclau
Patai's chemistry of functional groups (2024), pp. 1-56
Closed Access
Relating Conformational Equilibria to Conformer‐Specific Lipophilicities: New Opportunities in Drug Discovery
Bruno Linclau, Zhong Wang, Benjamin Jeffries, et al.
Angewandte Chemie (2021) Vol. 134, Iss. 7
Open Access | Times Cited: 3
Application of (4R)-aminoproline in peptide engineering: conformational bias and pH-responsiveness revisited
Vladimir Kubyshkin
New Journal of Chemistry (2022) Vol. 46, Iss. 20, pp. 9587-9594
Closed Access | Times Cited: 2
Impact of β-perfluoroalkyl substitution of proline on the proteolytic stability of its peptide derivatives
Anton V. Chernykh, Danylo Aloshyn, Yuliya O. Kuchkovska, et al.
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 47, pp. 9337-9350
Closed Access | Times Cited: 1
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