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Synthesis of 2‐(Trifluoromethyl)‐dibenzopyranones with Rhodium(III)‐catalyzed Formal anti‐Michael Addition as Key Step
Advanced Synthesis & Catalysis ( IF 5.4 ) Pub Date : 2018-01-15 , DOI: 10.1002/adsc.201701511
Ling Pan 1 , Jinhuan Dong 1, 2 , Di Xie 1 , Yifei Li 1 , Qun Liu 1
Affiliation  

A novel rhodium(III)‐catalyzed synthesis of 2‐(trifluoromethyl)‐dibenzopyranones from easily available 4‐(trifluoromethyl)‐p‐quinols and N‐methoxyarylamides is described. Rhodium(III)‐catalyzed formal anti‐Michael addition was proposed to be a crucial step in this [3+3] annulation with N‐methoxyarylamides as effective 1,3‐dipoles, providing a concise and efficient approach for the construction of trifluoromethyl‐containing dibenzopyranones under mild reaction conditions.

中文翻译:

铑(III)催化的正式抗迈克尔加成反应为关键步骤合成2-(三氟甲基)-二苯并吡喃酮

描述了一种新型的铑(III)催化的合成方法,它由易于获得的4-(三氟甲基)-苯二酚和N-甲氧基芳基酰胺合成2-(三氟甲基)-二苯并吡喃酮。铑(III)催化的正式反迈克尔加成反应是将N-甲氧基芳酰胺作为有效的1,3-偶极子进行[3 + 3]环化反应的关键步骤,为构造三氟甲基在温和的反应条件下含有二苯并吡喃酮。
更新日期:2018-01-15
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