Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Baylis–Hillman Adducts as a Versatile Module for Constructing Fluorogenic Release System
Lanning Zhao, Yuan Qu, Fang Zhang, et al.
Journal of Medicinal Chemistry (2022) Vol. 65, Iss. 8, pp. 6056-6069
Closed Access | Times Cited: 11

Showing 11 citing articles:

Molecule fluorescent probes for sensing and imaging analytes in plants: Developments and challenges
Xiaopeng Yang, Qian-Qian Zhang, Shiyi Zhang, et al.
Coordination Chemistry Reviews (2023) Vol. 487, pp. 215154-215154
Closed Access | Times Cited: 41
Fluorogenic Reactions in Chemical Biology: Seeing Chemistry in Cells
Yanyan Chen, Hao Jiang, Tingting Hao, et al.
Chemical & Biomedical Imaging (2023) Vol. 1, Iss. 7, pp. 590-619
Open Access | Times Cited: 36
Mechanism‐Guided Design of Chain‐Growth Click Polymerization Based on a Thiol‐Michael Reaction
Suqiu Jiang, Hanchu Huang
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 13
Closed Access | Times Cited: 17
Recent Progress on NIR Fluorescent Probes for Enzymes
Jintao Zhao, Tao Ma, Bingbing Chang, et al.
Molecules (2022) Vol. 27, Iss. 18, pp. 5922-5922
Open Access | Times Cited: 27
Puromycin Prodrug Activation by Thioredoxin Reductase Overcomes Its Promiscuous Cytotoxicity
Bingbing Chang, Qianhe Xu, Hairui Guo, et al.
Journal of Medicinal Chemistry (2023) Vol. 66, Iss. 5, pp. 3250-3261
Closed Access | Times Cited: 11
Tunable Stimuli-Responsive Module Based on α-Hydroxymethyl-α,β-Unsaturated Carbonyl Scaffold
Rongfeng Shen, Baoxin Zhang, Lanning Zhao, et al.
Journal of Materials Chemistry B (2025)
Closed Access
Glutathione‐triggered prodrugs: Design strategies, potential applications, and perspectives
Jintao Zhao, Xinming Li, Tao Ma, et al.
Medicinal Research Reviews (2023) Vol. 44, Iss. 3, pp. 1013-1054
Closed Access | Times Cited: 9
Targeting Cytotoxic Agents through EGFR-Mediated Covalent Binding and Release
Pasquale A. Morese, Nahoum G. Anthony, Michael S. Bodnarchuk, et al.
Journal of Medicinal Chemistry (2023) Vol. 66, Iss. 17, pp. 12324-12341
Open Access | Times Cited: 6
Synthesis and discovery of Baylis-Hillman adducts as potent and selective thioredoxin reductase inhibitors for cancer treatment
Yilin He, Miao Zhong, Zi‐Long Song, et al.
Bioorganic & Medicinal Chemistry (2023) Vol. 79, pp. 117169-117169
Closed Access | Times Cited: 3
Mechanism‐Guided Design of Chain‐Growth Click Polymerization Based on a Thiol‐Michael Reaction
Suqiu Jiang, Hanchu Huang
Angewandte Chemie (2023) Vol. 135, Iss. 13
Closed Access | Times Cited: 1
Ionic liquid Supported Quinuclidine Catalyzed Morita-Baylis-Hillman Reaction
Vivek Srivastava
Letters in Organic Chemistry (2023) Vol. 20, Iss. 12, pp. 1095-1104
Closed Access
Page 1

Scroll to top