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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:

Profiling Sulfur(VI) Fluorides as Reactive Functionalities for Chemical Biology Tools and Expansion of the Ligandable Proteome
Katharine Gilbert, Aini Vuorinen, Arron Aatkar, et al.
ACS Chemical Biology (2023) Vol. 18, Iss. 2, pp. 285-295
Open Access | Times Cited: 42

Showing 1-25 of 42 citing articles:

Emerging and Re-emerging Warheads for Targeted Covalent Inhibitors: An Update
Laura Hillebrand, Xiaojun Julia Liang, Ricardo Augusto Massarico Serafim, et al.
Journal of Medicinal Chemistry (2024) Vol. 67, Iss. 10, pp. 7668-7758
Closed Access | Times Cited: 39
Global Reactivity Profiling of the Catalytic Lysine in Human Kinome for Covalent Inhibitor Development
Guanghui Tang, Wei Wang, Chengjun Zhu, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 12
Closed Access | Times Cited: 12
Efficient Ligand Discovery Using Sulfur(VI) Fluoride Reactive Fragments
Arron Aatkar, Aini Vuorinen, Oliver Longfield, et al.
ACS Chemical Biology (2023) Vol. 18, Iss. 9, pp. 1926-1937
Open Access | Times Cited: 20
The expanding repertoire of covalent warheads for drug discovery
Namrashee V. Mehta, Mariam S. Degani
Drug Discovery Today (2023) Vol. 28, Iss. 12, pp. 103799-103799
Closed Access | Times Cited: 17
Proteome-wide structural analysis identifies warhead- and coverage-specific biases in cysteine-focused chemoproteomics
Matthew White, Jesús Gil, Edward W. Tate
Cell chemical biology (2023) Vol. 30, Iss. 7, pp. 828-838.e4
Open Access | Times Cited: 15
A modular flow platform for sulfur(VI) fluoride exchange ligation of small molecules, peptides and proteins
Miguel Bernús, Daniele Mazzarella, Jelena Stanić, et al.
Nature Synthesis (2023) Vol. 3, Iss. 2, pp. 185-191
Closed Access | Times Cited: 15
A chemoproteomic platform for selective deubiquitinase inhibitor discovery
Rosa Cookson, Aini Vuorinen, Jonathan Pettinger, et al.
Cell Reports Physical Science (2023) Vol. 4, Iss. 10, pp. 101636-101636
Open Access | Times Cited: 12
Stereoselective Fluorosulfonylation of Vinylboronic Acids for (E)-Vinyl Sulfonyl Fluorides with Copper Participation
Jianquan Hong, Chunxiang Li, Kui Zhao, et al.
Organic Letters (2024) Vol. 26, Iss. 11, pp. 2332-2337
Closed Access | Times Cited: 3
The Modular Synthesis of Sulfondiimidoyl Fluorides and their Application to Sulfondiimidamide and Sulfondiimine Synthesis
Mingyan Ding, Charles Bell, Michael C. Willis
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 38
Open Access | Times Cited: 3
Sulfur (VI) fluoride exchange (SuFEx): a versatile tool to profile protein-biomolecule interactions for therapeutic development
Lingyun Yang, Zhengnan Yuan, Yongkuan Li, et al.
Medicinal Chemistry Research (2024) Vol. 33, Iss. 8, pp. 1315-1329
Closed Access | Times Cited: 2
SuFEx Chemistry Enables Covalent Assembly of a 280-kDa 18-Subunit Pore-Forming Complex
Lee Schnaider, Sophia K. Tan, Pratik Raj Singh, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 36, pp. 25047-25057
Closed Access | Times Cited: 2
Mechanistic Modeling of Lys745 Sulfonylation in EGFR C797S Reveals Chemical Determinants for Inhibitor Activity and Discriminates Reversible from Irreversible Agents
Kemel Arafet, Laura Scalvini, Francesca Galvani, et al.
Journal of Chemical Information and Modeling (2023) Vol. 63, Iss. 4, pp. 1301-1312
Open Access | Times Cited: 7
Reactive fragments targeting carboxylate residues employing direct to biology, high-throughput chemistry
Ross P. Thomas, Emma K. Grant, Eleanor R. Dickinson, et al.
RSC Medicinal Chemistry (2023) Vol. 14, Iss. 4, pp. 671-679
Open Access | Times Cited: 7
Electrophile Scanning Reveals Reactivity Hotspots for the Design of Covalent Peptide Binders
Nathalie M. Grob, Clint Remarcik, Simon L. Rössler, et al.
ACS Chemical Biology (2023) Vol. 19, Iss. 1, pp. 101-109
Closed Access | Times Cited: 6
Targeting the ubiquitin system by fragment-based drug discovery
Cassandra R. Kennedy, Katherine McPhie, Katrin Rittinger
Frontiers in Molecular Biosciences (2022) Vol. 9
Open Access | Times Cited: 10
Activation-Free Sulfonyl Fluoride Probes for Fragment Screening
László Petri, Péter Ábrányi‐Balogh, Noémi Csorba, et al.
Molecules (2023) Vol. 28, Iss. 7, pp. 3042-3042
Open Access | Times Cited: 5
Cell-active, irreversible covalent inhibitors that selectively target the catalytic lysine of EGFR by using fluorosulfate-based SuFEx chemistry
Guanghui Tang, Wei Wang, Xuan Wang, et al.
European Journal of Medicinal Chemistry (2023) Vol. 259, pp. 115671-115671
Closed Access | Times Cited: 5
Organometallic Bridge Diversification of Bicyclo[1.1.1]pentanes
Joseph M. Anderson, Darren L. Poole, Gemma C. Cook, et al.
Chemistry - A European Journal (2023) Vol. 30, Iss. 12
Closed Access | Times Cited: 5
Enantioselective Synthesis of Chiral Sulfonimidoyl Fluorides Facilitates Stereospecific SuFEx Click Chemistry
He-sen Huang, Yi Yuan, Wei Wang, et al.
Angewandte Chemie (2024)
Open Access | Times Cited: 1
Target discovery of bioactive natural products with native-compound-coupled CNBr-activated Sepharose 4B beads (NCCB): Applications, mechanisms and outlooks
Yueteng Zhang, Junjie Zhang, Menglong Li, et al.
Bioorganic & Medicinal Chemistry (2023) Vol. 96, pp. 117483-117483
Closed Access | Times Cited: 4
Copper‐Mediated N‐Trifluoromethylation of O‐Benzoylhydroxylamines
Thomas D. Fleetwood, William J. Kerr, J. S. Mason
Chemistry - A European Journal (2023) Vol. 30, Iss. 6
Open Access | Times Cited: 4
Offsetting Low-Affinity Carbohydrate Binding with Covalency to Engage Sugar-Specific Proteins for Tumor-Immune Proximity Induction
Benjamin Lake, Anthony F. Rullo
ACS Central Science (2023) Vol. 9, Iss. 11, pp. 2064-2075
Open Access | Times Cited: 2
Covalent fragment libraries in drug discovery—Design, synthesis, and screening methods
Brad J. W. Hocking, Alan Armstrong, David J. Mann
Progress in medicinal chemistry (2023), pp. 105-146
Closed Access | Times Cited: 2
コバレントドラッグのための細胞内反応化学
Naoya Shindo, Akio Ojida
Journal of Synthetic Organic Chemistry Japan (2024) Vol. 82, Iss. 1, pp. 50-62
Closed Access
Reaction Space Charting as a Tool in Organic Chemistry Research and Development
Eloy Lozano Baró, Pau Nadal Rodríguez, Jordi Juárez‐Jiménez, et al.
Advanced Synthesis & Catalysis (2024) Vol. 366, Iss. 4, pp. 551-573
Open Access
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