Efficiently Constructing Tetrahydroquinolines through Cascade Radical Additions and Cyclizations under the Catalysis of Cu I

Abstract An efficient method has been developed for the construction of tetrahydroquinolines from N , N ‐dimethylanilines and electron‐deficient alkenes based on CuCl/O 2 . A wide scope of substrates could be well tolerated, and excellent yields of the products were obtained. A series of control experiments and kinetic isotope effect experiments have been performed to gain insight of the catalytic reaction pathway. The reaction is probably initiated by the reaction of Cu I and molecular oxygen to give copper(II) superoxide (Cu II OO . ) as the key reactive intermediate. The formed Cu II OO . species can directly abstract a hydrogen from the α ‐site of nitrogen to give the α ‐amino radical intermediate, which then finishes the transformation via radical addition and cyclization.