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

作者：Rohan Chandra Das, Soumen Barik, Anusree A. Kunhiraman, Anubhav Goswami, Avijit Mondal, Mrinmoy De, Akkattu T. Biju · 发表于：ACS Catalysis · 年份：2024 · DOI：10.1021/acscatal.4c00793 · 被引用次数：20 · 研究领域：N-Heterocyclic Carbenes in Organic and Inorganic Chemistry、Catalytic Cross-Coupling Reactions、Synthetic Organic Chemistry Methods

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 α-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.