A short scalable biomimetic route to bioactive natural product bimagnolignan () was accomplished. Compound was successfully prepared through a three-step metal-free synthesis from honokiol (). Alternatively, was also synthesized by biomimetic transformations that mimic tyrosinase in four steps. The key reactions feature a regioselective acetylation, a highly efficient C(sp)-H oxidation, a cascade aerobic oxidative cyclization/coupling, and a Cu-catalyzed direct oxidative coupling. In addition, cell-based assays validate that is a promising natural lead for HER2-positive breast cancer treatment.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1021/acs.orglett.4c00378 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!