Efficient synthesis of cyclic P-stereogenic phosphinamides from acyclic chiral precursors via radical oxidative intramolecular aryl C–H phosphinamidation

Abstract

We present a highly efficient method for the synthesis of cyclic P-stereogenic phosphinamides via the Ce^(IV)-promoted radical oxidative aryl C–H phosphinamidation of acyclic P-stereogenic phosphinamides. The new protocol provides a useful platform for the versatile synthesis of various potentially useful P-stereogenic compounds.