The NaIO 4 ‐promoted selenylation/cyclization of 1‐(2‐(vinyloxy)aryl)‐indoles with diselenides has been reported for the synthesis of selenized benzo5,61,4oxazino4,3‐ a indole derivatives. In this synthesis, the indole moiety with significant medicinal value, the morpholine skeleton, and the selenium group were introduced into a privileged structure, resulting in the target compound with potential value. The reaction features wide substrate scope, high group tolerance and good yield, which also represents the first selenylation/cyclization of 1‐(2‐(vinyloxy)aryl)‐indoles and diselenides.
Rong et al. (2026) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: