首页> 外文期刊>Journal of chemical research: reviews and research papers from all branches of chemistry >Facile synthesis of 2,2-bis(1 H-indol-3-yl)acenaphthen-1(2H)-one derivatives catalysed by ceric ammonium nitrate
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Facile synthesis of 2,2-bis(1 H-indol-3-yl)acenaphthen-1(2H)-one derivatives catalysed by ceric ammonium nitrate

机译:硝酸铈铵催化2,2-双(1 H-吲哚-3-基)ac啶-1(2H)-one衍生物的合成

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摘要

Ceric ammonium nitrate efficiently catalyses the reaction of acenaphthenequinone with indoles afforded symmetrical 2,2-bis(1H-indol-3-yl)acenaphthen-1(2H)-one in excellent yields within 2h under ethanol refluxing, as well as 2-hydroxy-2-indolylacenaphthen-1(2H)-one with indoles afforded the corresponding unsymmetrical 2,2-bis(1 H-indol3-yl)acenaphthen-1(2H)-one. This provides an efficient route to the synthesis of symmetrical and unsymmetrical 2,2-bis(1H-indol-3-yl)acenaphthen-1(2H)-one derivatives.
机译:硝酸铈铵可有效催化of啶醌与吲哚的反应,在乙醇回流下2小时之内即可获得对称的2,2-双(1H-吲哚-3-基)ac-1(2H)-一,且收率很高,而且2-羟基带有吲哚的-2-吲哚基苯甲酮-1(2H)-1提供了相应的不对称的2,2-双(1 H-吲哚3-基)ac庚烯-1(2H)-1。这为合成对称和不对称的2,2-双(1H-吲哚-3-基)ac啶-1(2H)-一衍生物提供了一条有效途径。

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