
ACS Catalysis, Год журнала: 2024, Номер 15(2), С. 817 - 827
Опубликована: Дек. 27, 2024
Transition metal catalysis is crucial for the synthesis of complex molecules, with ligands and bases playing a pivotal role in optimizing cross-coupling reactions. Despite advancements ligand design base selection, achieving effective synergy between these components remains challenging. We present here general approach to nickel-catalyzed photoredox reactions employing tert-butylamine as cost-effective bifunctional additive, acting ligand. This method proves C-O C-N bond-forming diverse array nucleophiles, including phenols, aliphatic alcohols, anilines, sulfonamides, sulfoximines, imines. Notably, protocol demonstrates significant applicability biomolecule derivatization facilitates sequential one-pot functionalizations. Spectroscopic investigations revealed robustness dynamic catalytic system, while elucidation structure-reactivity relationships demonstrated how computed molecular properties both nucleophile electrophile correlated reaction performance, providing foundation outcome prediction.
Язык: Английский