New and convergent synthesis of erdafitinib
Author:
Affiliation:
1. College of Chemistry and Chemical Engineering Shanghai University of Engineering Science Shanghai P.R. China
Publisher
Wiley
Subject
Organic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4544
Reference13 articles.
1. In vitro and in vivo evaluation of the radiosensitizing effect of a selective FGFR inhibitor (JNJ-42756493) for rectal cancer
2. Discovery and Pharmacological Characterization of JNJ-42756493 (Erdafitinib), a Functionally Selective Small-Molecule FGFR Family Inhibitor
3. Erdafitinib: First Global Approval
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1. Visible Light‐Promoted Mono‐Bromination of Aniline Derivatives and Nitrogen‐Containing Heterocyclic Compounds via Electron Donor‐Acceptor Complex;Asian Journal of Organic Chemistry;2024-07-25
2. A Streamlined, Green, and Sustainable Synthesis of the Anticancer Agent Erdafitinib;Organic Letters;2023-06-06
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