N-Heterocyclic Carbene-Catalyzed Imine Umpolung/Semipinacol Rearrangement Cascade for the Synthesis of Indoxyls

Aldimine umpolung using N-heterocyclic carbenes (NHCs) is less explored compared to the well-known polarity reversal of aldehydes. Described herein is the NHC-catalyzed aldimine umpolung/semipinacol rearrangement cascade for the atom- and pot-economic synthesis of fluorescent active, N-H unprotected indoxyl derivatives. Moreover, conditions are identified for the NHC-catalyzed enantioselective synthesis of alpha-iminols by the umpolung of aldimines. The nucleophilic aza-Breslow intermediates are intercepted with carbonyl electrophiles. Preliminary DFT studies shed light on the rearomative proton transfer coupled aryl migration in an ortho-quinonemethide intermediate facilitating the semipinacol rearrangement. In addition, the antibacterial activity of the synthesized indoxyls has been evaluated.