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Updated: Jul 27, 2025

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
A Streamlined, Green, and Sustainable Synthesis of the Anticancer Agent Erdafitinib
Vani Singhania1, Chandler B Nelson1, Maya Reamey1
1†Department of Chemistry and Biochemistry, University of California, Santa Barbara, California 93106, United States.
Abstract:
Erdafitinib, an anticancer drug, was synthesized in a three-step two-pot sequence involving ppm levels of Pd catalyst run under aqueous micellar conditions enabled by a biodegradable surfactant. This process features both pot- and time-economies and eliminates egregious organic solvents and toxic reagents associated with existing routes.
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