Diastereoselective construction of 3-aryl-substituted indolines <i>via</i> annulation of <i>in situ</i> generated <i>p</i>-quinone methides

Abstract

A highly diastereoselective [4 + 1] annulation reaction of in situ generated p-quinone methides for the synthesis of 3-aryl-substituted indolines has been developed. Employing commercial manganese dioxide as the oxidant, a series of ortho-tosylaminophenyl-substituted p-QMs could be generated in situ. This new protocol is based on an unprecedented 1,6-conjugate addition/annulation cascade reaction, without the need for pre-synthesized p-QMs, and enables the easy preparation of a variety of 3-aryl-2,3-dihydroindoles in good to excellent yields.