首页> 外文期刊>RSC Advances >An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)–H bond activation mediated by Selectfluor
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An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)–H bond activation mediated by Selectfluor

机译:由Selectfluor介导的C(sp3)–H键激活,由苯乙酮和蒽醌合成高效的3-酰基喹啉

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摘要

An efficient method for the synthesis of 3-functionalized quinolines from commercially available acetophenones and anthranil has been described. Selectfluor propels the C(sp ~(3) )–H bond activation of the acetophenones and aza-Michael addition of anthranil resulting in annulated 3-acylquinolines in moderate to high yields. DMSO acts not only as a solvent but also as a one carbon donor in the reaction.
机译:已经描述了从市售的苯乙酮和蒽醌合成3-官能化喹啉的有效方法。 Selectfluor推动了苯乙酮的C(sp〜(3))–H键活化和蒽酮的aza-Michael加成反应,从而制得了中度至高产率的环状3-酰基喹啉。 DMSO在反应中不仅充当溶剂,而且充当一个碳供体。

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