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Synthesis of functionalized 4-nitroanilines by ring transformation of dinitropyridone with enaminones
Tetrahedron Letters ( IF 1.5 ) Pub Date : 2017-11-03 , DOI: 10.1016/j.tetlet.2017.11.003
Saki Naito , Soichi Yokoyama , Haruyasu Asahara , Nagatoshi Nishiwaki

2-Functionalized 4-nitroanilines were readily synthesized by ring transformation using 3,5-dinitro-2-pyridone and enaminones prepared from 1,3-dicarbonyl compounds and amines. Modification of the amino group and the ortho-position could be achieved by simply changing the enaminones. Using this strategy, functional groups such as acetyl, benzoyl, and ethoxycarbonyl groups could be introduced into the nitroaniline framework.



中文翻译:

二硝基吡啶酮与烯胺酮的环转化合成功能化的4-硝基苯胺

通过使用由1,3-二羰基化合物和胺制备的3,5-二硝基-2-吡啶酮和烯胺酮,通过环转化,可以轻松合成2-官能化的4-硝基苯胺。氨基和位的修饰可以通过简单地改变烯胺酮来实现。使用这种策略,可以将诸如乙酰基,苯甲酰基和乙氧羰基的官能团引入硝基苯胺框架中。

更新日期:2017-11-03
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