SILP catalyst with grafted pyridinium ions was used for either mono- or double carbonylation depending on the reaction conditions. Good recyclability and low palladium loss were observed during the synthesis of pharmaceutically active compounds.
A Ni-catalyzed cross coupling of arylzinc reagents with pyridinium ions provides enantioenriched dihydropyridines, which are precursors to diverse piperidine derivatives.
The reactivity of pyridinium ions was utilized for the first non-precious-metal-catalyzed C-3 direct arylation and was demonstrated by mechanistic studies.