Enantioselective Organophotocatalytic α-Functionalization of Aldehydes with N-Lactam Radicals: A Viable Strategy for the Telescoped Synthesis of Levetiracetam
Articolo
Data di Pubblicazione:
2025
Citazione:
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]
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.
Tipologia IRIS:
01 - Articolo su periodico
Keywords:
Aldehydes; Chemical reactions; Enantioselective synthesis; Organocatalysts; Precursors;
Elenco autori:
E. Colombo, M.F. Boselli, M. Fattalini, V. Chiroli, S. Rossi, M. Benaglia, A. Puglisi
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