Nickel-catalysed para-CH activation of pyridine with switchable regioselective hydroheteroarylation of allylarenes

Abstract

para-CH activation of pyridine with allylbenzene is described by Ni/Al cooperative catalysis in combination with a bulkier NHC ligand and a Lewis acid, leading to linear hydroheteroarylation products. Interestingly, the branch selectivity can be achieved by using the combination of a less sterically hindered amino-NHC ligand and AlMe₃ through tandem reaction of facile alkene isomerization followed by a slow CH bond activation process.