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首页> 外文期刊>Journal of Organometallic Chemistry >Synthesis of bis(indolyl) alkanes by a site-selective gold-catalyzed addition of indoles to butynol derivatives
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Synthesis of bis(indolyl) alkanes by a site-selective gold-catalyzed addition of indoles to butynol derivatives

机译:通过位点选择性金催化的吲哚向丁炔醇衍生物的加成反应合成双(吲哚基)烷烃

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摘要

A new site-selective hydroarylation reaction of alkynes catalyzed by gold complexes and directed by an internal hydroxyl group has been developed. Thus, the treatment of 3-butyn-1-ol derivatives with indoles and a catalytic amount of an in situ formed cationic gold complex leads to the formation of bis(indolyl) alkane derivatives. Particularly interesting is the reaction with terminal alkynes as the double addition of the indol occurs at the terminal carbon of the triple bond. The reaction conditions are very mild and the final bis(indolyl) alkanes are obtained in high yields. (C) 2008 Elsevier B.V. All rights reserved.
机译:已经开发了一种新的由金配合物催化并由内部羟基引导的炔烃的位点选择性加氢芳基化反应。因此,用吲哚和催化量的原位形成的阳离子金络合物处理3-丁炔-1-醇衍生物导致双(吲哚基)烷烃衍生物的形成。特别令人感兴趣的是与末端炔烃的反应,因为吲哚的双重加成发生在三键的末端碳上。反应条件非常温和,最终双(吲哚基)烷烃的收率很高。 (C)2008 Elsevier B.V.保留所有权利。

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