Flavin‐Catalyzed Aerobic Oxidative C−C Bond Formation by Metal/Light‐Free Cross‐Dehydrogenative Coupling
Biomimetic flavin catalysts enable green and selective aerobic oxidative transformations. However, most previous studies tended to focus on reproducing the enzymatic function of flavin monooxygenase, thereby limiting the applications of flavin catalysts to oxygen‐atom transfer reactions. We herein r...
Gespeichert in:
Veröffentlicht in: | Advanced synthesis & catalysis 2024-02, Vol.366 (3), p.402-407 |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | Biomimetic flavin catalysts enable green and selective aerobic oxidative transformations. However, most previous studies tended to focus on reproducing the enzymatic function of flavin monooxygenase, thereby limiting the applications of flavin catalysts to oxygen‐atom transfer reactions. We herein report a cross‐dehydrogenative coupling (CDC) between the sp3 C−H bond of tetrahydroisoquinolines and the sp3 and sp2 C−H bonds of carbon nucleophiles, such as α‐methylene carbonyl compounds, nitromethane, and indoles, for C−C bond formation promoted by flavin catalysts. Flavin catalysis enables the oxidative C−H activation of tetrahydroisoquinolines and the efficient activation of molecular oxygen (1 atm) under mild and metal/light‐free conditions, thus facilitating a green aerobic CDC that generates benign water as the sole by‐product. |
---|---|
ISSN: | 1615-4150 1615-4169 |
DOI: | 10.1002/adsc.202301427 |