Dimedone-catalyzed Addition of Amines into Cyano Group: Facile Synthesis of Thiazol-2-yl Substituted E-Acrylonitriles

An efficient dimedone-catalyzed synthesis of highly functionalized thiazol-2-yl substituted E-acrylonitrile derivatives has been established through two-step reaction of a-thiocyanate ketones with malononitrile and amines. The a-thiocyanate ketones were subjected with malononitrile to provide thiazo...

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Veröffentlicht in:Chinese journal of chemistry 2012-07, Vol.30 (7), p.1617-1623
1. Verfasser: 朱伟军 屠兴超 冯惠 屠蔓苏 姜波 吴飞跃 屠树江
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container_title Chinese journal of chemistry
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creator 朱伟军 屠兴超 冯惠 屠蔓苏 姜波 吴飞跃 屠树江
description An efficient dimedone-catalyzed synthesis of highly functionalized thiazol-2-yl substituted E-acrylonitrile derivatives has been established through two-step reaction of a-thiocyanate ketones with malononitrile and amines. The a-thiocyanate ketones were subjected with malononitrile to provide thiazol-2-ylidenemalononitrile derivatives, followed with various amines in the presence of dimedone to yield the final thiazol-2-yl substituted acrylonitrile derivatives.
doi_str_mv 10.1002/cjoc.201100719
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subjects addition reaction
dimedone-catalyzed synthesis
E-acrylonitriles
heterocycles
microwave heating
丙烯腈
两步反应
催化合成
噻唑
氰基

衍生物

title Dimedone-catalyzed Addition of Amines into Cyano Group: Facile Synthesis of Thiazol-2-yl Substituted E-Acrylonitriles
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