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Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor.
Beilstein Journal of Organic Chemistry ( IF 2.2 ) Pub Date : 2020-07-17 , DOI: 10.3762/bjoc.16.144
Dalel El-Marrouki 1, 2 , Sabrina Touchet 1 , Abderrahmen Abdelli 2 , Hédi M'Rabet 2 , Mohamed Lotfi Efrit 2 , Philippe C Gros 1
Affiliation  

A convergent strategy is reported for the construction of nitrogen-containing heterocycles from common substrates: 1,4-diketones and primary amines. Indeed, by just varying the substrates, the substituents, or the heating mode, it is possible to selectively synthesize indole, indolone (1,5,6,7-tetrahydroindol-4-one), or cinnoline (5,6,7,8-tetrahydrocinnoline) derivatives in moderate to excellent yields.

中文翻译:


从常见的 1,4-二酮迈克尔受体可调节地获取吲哚、吲哚酮和肉桂啉衍生物。



据报道,从共同底物:1,4-二酮和伯胺构建含氮杂环的收敛策略。事实上,仅通过改变底物、取代基或加热模式,就可以选择性合成吲哚、吲哚酮(1,5,6,7-四氢吲哚-4-酮)或肉啉(5,6,7, 8-四氢肉啉)衍生物,产率中等至优异。
更新日期:2020-07-17
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