A metal-free and efficient visible-light-induced spirocyclization of indolyl-ynones with diselenides at room temperature under air atmosphere to prepare 3-selenospiroindolenines in moderate to good yields has been developed. The resulting products were tested for in vitro anticancer activity by MTT assay, and compounds 3 c and 3 e showed potent cancer cell-growth inhibition activities.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/asia.202000298 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!