Transient imine as a directing group for the Pd-catalyzed anomeric C(sp 3 )-H arylation of 3-aminosugars.

The first example of Pd(II)-catalyzed anomeric arylation of 3-aminosugars is reported by using an L,X-type transient directing group (TDG) approach combined with an external 2-pyridone ligand. The released free amine was in situ transformed into an azide function, which was then exploited in a CuAAC to increase the molecular complexity and prepare a variety of complex substituted C3-triazolo C -glycosides in good yields.