Palladium-catalyzed gaseous CO-free carbonylative C–C bond activation of cyclobutanones†
Abstract
A palladium-catalyzed carbonylative C–C bond activation reaction of cyclobutanones proceeding by C–C bond cleavage, ring-opening, and amino- or alkoxycarbonylation is reported here. Two C–C bonds and one C–O or C–N bond are created to afford a variety of indanones bearing ester or amide groups under gas-free conditions by using phenyl formate and benzene-1,3,5-triyl triformate (TFBen) as convenient CO surrogates.