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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives promoted by Ca(OTf)(2)
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A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives promoted by Ca(OTf)(2)

机译:Ca(OTf)(2)促进的立体选择性合成丙烯酸衍生物的简便一锅多米诺反应

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摘要

A facile one-pot domino reaction for the stereoselective synthesis of acryl derivatives has been reported using alkaline earth catalyst [Ca(OTf)(2)]. Initially aryl amine reacts with ethyl propiolate to form 6-enamino ester which further reacts with aryl aldehyde and indole in the presence of Ca(OTf)(2) to give indolyl acrylates. It is interesting to note that in the absence of indole the reaction leads to the formation of benzylidene bisacrylates. Similarly 6-enamino ester reacts with another electrophilic partner isatin in the presence of Ca(OTf)(2) to give oxindolyl acrylates. The products were isolated in good yields by simple filtration. (C) 2016 Elsevier Ltd. All rights reserved.
机译:据报道,使用碱土金属催化剂[Ca(OTf)(2)]可以轻松进行一锅多米诺骨牌反应,实现丙烯酸衍生物的立体选择性合成。最初,芳基胺与丙酸乙酯反应形成6-烯氨基酯,后者在Ca(OTf)(2)存在下进一步与芳基醛和吲哚反应,生成丙烯酸吲哚酯。有趣的是,在没有吲哚的情况下,该反应导致形成亚苄基双丙烯酸酯。类似地,6-烯氨基酯在Ca(OTf)(2)的存在下与另一种亲电子伴侣靛红反应,得到丙烯酸羟吲哚酯。通过简单过滤以高收率分离出产物。 (C)2016 Elsevier Ltd.保留所有权利。

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