首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >One-pot efficient green synthesis of spirooxindole-annulated thiopyran derivatives via Knoevenagel condensation followed by Michael addition
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One-pot efficient green synthesis of spirooxindole-annulated thiopyran derivatives via Knoevenagel condensation followed by Michael addition

机译:通过Knoevenagel缩合然后进行迈克尔加成反应,一锅高效地绿色合成螺并吲哚环化的噻喃衍生物

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摘要

A green, operationally simple and highly efficient one-pot three-component approach for the synthesis of spiro[indoline-3,4'-thiopyrano[2,3-b]indole] derivatives has been developed by the domino reaction of indoline-2-thione, isatin and ethyl cyanoacetate or malononitrile in ethanol at 80 °C for just 20 min. The significant advantages of this protocol are short reaction time, excellent yields, operational simplicity and formation of three new bonds in one operation from easily available starting materials.
机译:通过吲哚啉-2的多米诺反应,开发了一种绿色,操作简单且高效的一锅三组分合成螺[吲哚啉-3,4'-硫代吡喃并[2,3-b]吲哚]衍生物的方法。 -硫酮,靛红和氰基乙酸乙酯或丙二腈在80°C的乙醇中仅20分钟。该方案的显着优点是反应时间短,产率高,操作简便,并且一次操作中由容易获得的起始原料形成了三个新的键。

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