Rh(III)‐Catalyzed Selective C−H Alkylation and Alkenylation of 1,2,3‐Benzotriazinones with Maleimides
Herein, we describe a reaction conditions‐based switchable Rh(III)‐catalyzed C−H alkylation and alkenylation of 1,2,3‐benzotriazinones with maleimides, where the triazinone serves as a directing group rather than its traditional role denitrogenative precursor. This strategy enables the selective syn...
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Veröffentlicht in: | Advanced synthesis & catalysis 2024-09, Vol.366 (17), p.3646-3652 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Herein, we describe a reaction conditions‐based switchable Rh(III)‐catalyzed C−H alkylation and alkenylation of 1,2,3‐benzotriazinones with maleimides, where the triazinone serves as a directing group rather than its traditional role denitrogenative precursor. This strategy enables the selective synthesis of diverse 3‐arylated succinimides and 3‐arylated maleimides in up to 99% yield and a broad substrate scope (48 examples). Furthermore, for the first time, a tandem C−H alkylation and denitrogenative coupling of 1,2,3‐benzotriazinones has been achieved by slightly modifying the reaction conditions. Additionally, gram‐scale reactions and product derivatizations were conducted to demonstrate the synthetic utility. |
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ISSN: | 1615-4150 1615-4169 |
DOI: | 10.1002/adsc.202400410 |