铑(III)催化苯甲亚胺酸乙酯和CF3-亚胺氧锍叶立德C—H 活化/环化反应合成CF3-1H-苯并[de][1,8]萘吡啶
收稿日期: 2023-06-01
修回日期: 2023-07-26
网络出版日期: 2023-08-22
基金资助
国家自然科学基金(22071068); 及华侨大学分析测试中心资助项目.
Rhodium(III)-Catalyzed Synthesis of CF3-1H-benzo[de][1,8]naph-thyridines via C—H Activation/Annulation of Benzimidates and CF3-Imidoyl Sulfoxonium Ylides
Received date: 2023-06-01
Revised date: 2023-07-26
Online published: 2023-08-22
Supported by
National Natural Science Foundation of China(22071068); Instrumental Analysis Center of Huaqiao University.
在铑催化下, 实现了苯甲亚胺酸乙酯类化合物与CF3-亚胺叶立德的C—H活化/环化多米诺反应. 该合成策略具有良好的官能团耐受性和底物的普适性, 合成了一系列含三氟甲基的1H-苯并[de][1,8]萘吡啶, 产率为22%~86%.
关键词: 铑催化; 苯甲胺酸乙酯; 三氟甲基; 氧锍叶立德; 苯并[de][1,8]萘吡啶
文思 , 丁宇浩 , 田青于 , 葛进 , 程国林 . 铑(III)催化苯甲亚胺酸乙酯和CF3-亚胺氧锍叶立德C—H 活化/环化反应合成CF3-1H-苯并[de][1,8]萘吡啶[J]. 有机化学, 2024 , 44(1) : 291 -300 . DOI: 10.6023/cjoc202306002
A rhodium-catalyzed C—H activation/annulation domino reaction of benzimidates and CF3-imidoyl sulfoxonium ylides has been achieved. This synthetic strategy has good functional groups tolerance and universality of substrates, and a series of trifluoromethyl-containing 1H-benzo[de][1,8]naphthyridines were synthesized in 22%~86% yields.
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