Affiliation:
1. Engineering Research Centre of Pharmaceutical Process Chemistry Ministry of Education School of Pharmacy East China University of Science and Technology 130 Meilong Road Shanghai 200237 P. R. China .
Abstract
AbstractVarious indoles and carbazoles were synthesized from o‐alkenyl anilines and o‐aryl anilines by the β‐C(sp2)−H bond amination cyclization without any oxidants or hydrogen acceptors. Likewise, employing o‐alkyl anilines as substrates, indole products are also obtained by the β‐C(sp3)−H bond amination cyclization, and dehydrogenation. In this cross‐dehydrogenative coupling, many different functional groups are tolerated, and hydrogen gas is the only by‐product, thereby providing an intrinsically waste‐free approach for the synthesis of indoles and carbazoles.
Funder
National Natural Science Foundation of China