The mild photocatalytic generation of N-lactam radicals is explored for the enantioselective α-functionalization of aldehydes in the presence of a chiral imidazolidinone organocatalyst. The reaction provides the desired products in high yields and up to 92% ee using a structurally simple, low-cost, and easy-to-prepare organocatalyst. The methodology was successfully applied to the telescoped synthesis of a pharmacologically relevant compound, (S)-levetiracetam, an antiepileptic drug.
Enantioselective Organophotocatalytic α-Functionalization of Aldehydes with N-Lactam Radicals: A Viable Strategy for the Telescoped Synthesis of Levetiracetam / E. Colombo, M.F. Boselli, M. Fattalini, V. Chiroli, S. Rossi, M. Benaglia, A. Puglisi. - In: ORGANIC LETTERS. - ISSN 1523-7060. - (2025), pp. 1-5. [10.1021/acs.orglett.5c02365]
Enantioselective Organophotocatalytic α-Functionalization of Aldehydes with N-Lactam Radicals: A Viable Strategy for the Telescoped Synthesis of Levetiracetam
E. ColomboCo-primo
Membro del Collaboration Group
;M.F. BoselliCo-primo
Membro del Collaboration Group
;M. FattaliniSecondo
Membro del Collaboration Group
;V. ChiroliMembro del Collaboration Group
;S. RossiSupervision
;M. BenagliaPenultimo
Supervision
;A. Puglisi
Ultimo
Supervision
2025
Abstract
The mild photocatalytic generation of N-lactam radicals is explored for the enantioselective α-functionalization of aldehydes in the presence of a chiral imidazolidinone organocatalyst. The reaction provides the desired products in high yields and up to 92% ee using a structurally simple, low-cost, and easy-to-prepare organocatalyst. The methodology was successfully applied to the telescoped synthesis of a pharmacologically relevant compound, (S)-levetiracetam, an antiepileptic drug.| File | Dimensione | Formato | |
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