Herein, we describe the development of a copper-catalyzed C(sp3)-amination of proaromatic dihydroquinazolinones derived from ketones. The reaction is enabled by the intermediacy of open-shell species arising from homolytic C−C bond-cleavage driven by aromatization. The protocol is characterized by its operational simplicity and generality, including chemical diversification of advanced intermediates.
Article
Versió publicada
Anglès
6 p.
Wiley-VCH
FEDER/MCI PID2021-123801NB-I00
China Scholarship Council (CSC)
European Research Council (ERC) under European Union's Horizon 2020 research and innovation program (grant agreement No 883756)
Creative Commons. Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0)
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