Acylative Suzuki coupling of amides: acyl-nitrogen activation via synergy of independently modifiable activating groups

Chem Commun (Camb). 2015 Mar 25;51(24):5089-92. doi: 10.1039/c5cc00430f.

Abstract

A highly efficient palladium-catalyzed acylative cross-coupling of carboxylic amides with arylboronic acids has been achieved via synergistic activation of the C(acyl)-N bond by independently modifiable activating groups. Coupling of amides features not only good functional group tolerance but also modifiable reactivities to overcome steric hindrance.