Palladium-catalyzed hydroamination yields high enantioselectivity in pyridone derivatives, suggesting advancements in organic synthesis.
A palladium-catalyzed reaction for the hydroamination of alkoxyallenes with 2-pyridones has been developed. This method is highly chemo-, regio-, and enantioselective, providing efficient access to pyridone-containing N,O-acetals in excellent yields (up to 98%) and enantioselectivity (up to 99% ee). DFT mechanistic studies reveal that enantiocontrol originates in the rate-determining proton transfer step, where dual hydrogen-bonding interactions between the diphosphine ligand's amide group, the alkoxyallene, and the 2-pyridone substrate favor the formation of the (S)-configured N,O-acetal product.
No takes yet. Share an insight, caveat, or question.
Xu et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: