A rhodium-catalyzed
cyclization of azobenzenes and vinylene carbonate
via C–H bond activation to construct indazolo[2,3-a]quinolines has been developed. This protocol offers an efficient
method for synthesis of the titled products in good yields with broad
functional group tolerance. In this reaction, three C–C bonds
and C–N bond are formed in one pot, and vinylene carbonate
(VC) acts as C1 and C2 synthons as well as “vinylene transfer”
agent and acylation reagent in the construction of target-fused heterocycles.
Moreover, the products exhibit favorable fluorescence properties,
which indicate their potential application as fluorescent materials
and biosensors