We report the generation of N-oxazolidinone radicals via electron donor–acceptor (EDA) complex formation. Visible light irradiation of pyridinium-based radical precursors, either in the presence or in the absence of NaHCO3, enables a mild, regioselective and operationally simple N-arylation, providing direct access to N-aryloxazolidin-2-ones. The transformation can be easily converted into a continuous flow process, providing improved productivity over the corresponding batch reaction.
Visible-light-induced regioselective N-oxazolidinone radical addition to indoles and arenes via EDA complex formation / M.F. Boselli, S. Ferrario, N. Intini, K. Zeitler, A. Puglisi. - In: ORGANIC & BIOMOLECULAR CHEMISTRY. - ISSN 1477-0539. - (2026). [10.1039/d6ob00369a]
Visible-light-induced regioselective N-oxazolidinone radical addition to indoles and arenes via EDA complex formation
M.F. BoselliCo-primo
;S. FerrarioCo-primo
;A. Puglisi
Ultimo
2026
Abstract
We report the generation of N-oxazolidinone radicals via electron donor–acceptor (EDA) complex formation. Visible light irradiation of pyridinium-based radical precursors, either in the presence or in the absence of NaHCO3, enables a mild, regioselective and operationally simple N-arylation, providing direct access to N-aryloxazolidin-2-ones. The transformation can be easily converted into a continuous flow process, providing improved productivity over the corresponding batch reaction.| File | Dimensione | Formato | |
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