A novel Cp*RhCl2-catalyzed cyclization produces carbazoles from vinylindoles, suggesting efficient synthesis methods.
A [Cp*RhCl2]2-catalyzed formal [5+1] cyclization of 3-vinylindoles with diazo compounds has been developed for the synthesis of functionalized carbazoles. This strategy involves sequential C-H insertion, Claisen condensation, and aromatization. The advantages of this strategy include easy operation, good yields, mild conditions, and good functional group tolerance.
No takes yet. Share an insight, caveat, or question.
Xing et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: