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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Xiao et al. (2024) studied this question.
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