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首页> 外文期刊>Angewandte Chemie >Formation of Enehydrazine Intermediates through Coupling of Phenylhydrazines with Vinyl Halides: Entry into the Fischer Indole Synthesis
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Formation of Enehydrazine Intermediates through Coupling of Phenylhydrazines with Vinyl Halides: Entry into the Fischer Indole Synthesis

机译:通过苯肼与乙烯基卤化物的偶联形成中间体肼苯肼:进入费歇尔吲哚合成

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摘要

Indoles, one of the most abundant heterocycles in nature, constitute the essential functional cores in the structures of various fragrances, dyes, agricultural chemicals, and pharmaceuticals. The synthesis of indoles has been an active research field because of their structural diversity as well as the numerous applications of natural and synthetic indole derivatives. Over the last century, a wide array of approaches have been developed, and among them the Fischer indole synthesis is probably the most well-known method because of its fascinating combination of experimental simplicity and mechanistic complexity. Although it was established over a century ago in 1883, the Fischer indole synthesis still remains a popular research topic and substantial efforts have been made to explore its applications or to overcome its drawbacks.
机译:吲哚是自然界中最丰富的杂环之一,构成了各种香料,染料,农药和药物结构中必不可少的功能核心。吲哚的合成由于其结构的多样性以及天然和合成吲哚衍生物的众多应用而一直是活跃的研究领域。上个世纪以来,已经开发出了各种各样的方法,其中Fischer吲哚合成可能是最著名的方法,因为它将实验简单性和机械复杂性完美地结合在一起。尽管费希尔吲哚合成法建立于一个多世纪前的1883年,但它仍然是一个热门的研究主题,并且已经进行了大量努力来探索其应用或克服其缺点。

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