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Silyl palladium cations (R3P)2Pd–SiR3+ catalyze the ring opening, C–C bond forming, and functionalization of 5- and 6-membered cyclic allyl ethers with O-silyl nucleophiles. Conditions for high regio-control are achieved by adjustments in the phosphine electronics, with the identity of the 2-substituent also influencing the functionalization location in unsymmetrical furans. Allyl alcohols are obtained with a regio-preference for terminal addition with unsubstituted ethers with E-products being obtained with XantPhos and Z- with (4-CF3–Ar)3 ligation. Styrenes dominate with phenyl-substituted dihydrofurans, and for 2-alkyl-substituted, secondary alcohols result from an allyl migration pathway. Mechanistic studies demonstrate the feasibility of Pd–Si+ bonds to facilitate C–O activation to yield π-allyl intermediates, and for one substrate class to also sequence π-allyl migration prior to nucleophilic addition. DFT calculations demonstrated the viability of silylium-activated ether as a competent ligand for Pd(0).