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:

Synthesis of Chiral Triazole-Based Halogen Bond Donors
Mikk Kaasik, Sandra Kaabel, Kadri Kriis, et al.
Synthesis (2019) Vol. 51, Iss. 10, pp. 2128-2135
Closed Access | Times Cited: 20

Showing 20 citing articles:

Catalysis of Organic Reactions through Halogen Bonding
Revannath L. Sutar, Stefan M. Huber
ACS Catalysis (2019) Vol. 9, Iss. 10, pp. 9622-9639
Closed Access | Times Cited: 377

σ‐Hole Interactions in Catalysis
Martin Breugst, Jonas J. Koenig
European Journal of Organic Chemistry (2020) Vol. 2020, Iss. 34, pp. 5473-5487
Open Access | Times Cited: 174

Recognition in the Domain of Molecular Chirality: From Noncovalent Interactions to Separation of Enantiomers
Paola Peluso, Bezhan Chankvetadze
Chemical Reviews (2022) Vol. 122, Iss. 16, pp. 13235-13400
Closed Access | Times Cited: 170

Bidentate Chiral Bis(imidazolium)‐Based Halogen‐Bond Donors: Synthesis and Applications in Enantioselective Recognition and Catalysis
Revannath L. Sutar, Elric Engelage, Raphael Stoll, et al.
Angewandte Chemie International Edition (2020) Vol. 59, Iss. 17, pp. 6806-6810
Open Access | Times Cited: 95

Fine‐Tuning Substrate–Catalyst Halogen–Halogen Interactions for Boosting Enantioselectivity in Halogen‐Bonding Catalysis
Alica C. Keuper, Kevin Fengler, Florian Ostler, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 35
Open Access | Times Cited: 27

Neutral Chiral Tetrakis‐Iodo‐Triazole Halogen‐Bond Donor for Chiral Recognition and Enantioselective Catalysis
Florian Ostler, Dariusz G. Piekarski, Tobias Danelzik, et al.
Chemistry - A European Journal (2020) Vol. 27, Iss. 7, pp. 2315-2320
Open Access | Times Cited: 38

Intramolecular Nicholas Reactions in the Synthesis of Heteroenediynes Fused to Indole, Triazole, and Isocoumarin
Natalia A. Danilkina, Alexander S. D’yachenko, Anastasia I. Govdi, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 14, pp. 9001-9014
Closed Access | Times Cited: 22

Chiral Ferrocenyl−Iodotriazoles and −Iodotriazoliums as Halogen Bond Donors. Synthesis, Solid State Analysis and Catalytic Properties.
Emmanuel Aubert, Abdelatif Doudouh, Emmanuel Wenger, et al.
European Journal of Inorganic Chemistry (2022) Vol. 2022, Iss. 5
Open Access | Times Cited: 13

Hydrogen Bond-Enhanced Halogen Bonding Organocatalyst with C(sp3)–Br and Sulfoxide Moieties
Yuheng Zhang, Haimeng Zhu, Boyuan Zhang, et al.
ACS Catalysis (2023) Vol. 13, Iss. 10, pp. 7103-7109
Closed Access | Times Cited: 7

Tunable chiral triazole-based halogen bond donors: assessment of donor strength in solution with nitrogen-containing acceptors
A. R. Peterson, Mikk Kaasik, Andrus Metsala, et al.
RSC Advances (2019) Vol. 9, Iss. 21, pp. 11718-11721
Open Access | Times Cited: 20

5-Iodo-1H-1,2,3-triazoles as Versatile Building Blocks
Ирина А. Балова, Natalia A. Danilkina, Anastasia I. Govdi
Synthesis (2020) Vol. 52, Iss. 13, pp. 1874-1896
Closed Access | Times Cited: 19

Zweizähnige chirale Bis(imidazolium)‐basierte Halogenbrückendonoren: Synthese und Anwendungen in enantioselektiver Erkennung und Katalyse
Revannath L. Sutar, Elric Engelage, Raphael Stoll, et al.
Angewandte Chemie (2020) Vol. 132, Iss. 17, pp. 6872-6877
Open Access | Times Cited: 17

Halogen Bond‐Catalyzed Friedel−Crafts Reactions of Furans Using a 2,2’‐Bipyridine‐Based Catalyst
Huimiao Zhang, Patrick H. Toy
Advanced Synthesis & Catalysis (2020) Vol. 363, Iss. 1, pp. 215-221
Closed Access | Times Cited: 14

Regioselective Synthesis of Halotriazoles and their Utility in Metal Catalyzed Coupling Reactions
Santosh J. Gharpure, Sudi Naveen, Rupali S. Chavan, et al.
European Journal of Organic Chemistry (2020) Vol. 2020, Iss. 44, pp. 6870-6886
Closed Access | Times Cited: 10

A new halogen bonding 1,2-iodo-triazolium-triazole benzene motif for anion recognition
Thanthapatra Bunchuay, Andrew Docker, Nicholas G. White, et al.
Polyhedron (2021) Vol. 209, pp. 115482-115482
Open Access | Times Cited: 9

Halogen Bonding in Organocatalysis
Revannath L. Sutar
(2021), pp. 269-305
Closed Access | Times Cited: 8

6-Aminocoumarin-derived Schiff base gelators: aggregation and sensing of CN, Fe3+, Cu2+ and CO2 under different conditions
E. Paul, Rameez Raza, Subrata Ranjan Dhara, et al.
RSC Advances (2024) Vol. 14, Iss. 45, pp. 32759-32770
Open Access

Catalysis by Halogen Bonding Based on Iodine
Revannath L. Sutar, Stefan M. Huber
(2022), pp. 27-67
Closed Access | Times Cited: 2

Exploration of Halogen Bonding for the Catalysis of Organic Reactions
Revannath L. Sutar, Stefan M. Huber
Supramolecular Catalysis (2021), pp. 413-426
Closed Access

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