首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Convenient Synthesis of 2-Amino-4H-chromenes from Photochemically Generated o-Quinone Methides and Malononitrile
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Convenient Synthesis of 2-Amino-4H-chromenes from Photochemically Generated o-Quinone Methides and Malononitrile

机译:从光化学生成的邻醌甲基丙二酸和丙二腈方便地合成2-氨基-4H-色烯

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摘要

2-Amino-4H-chromenes were synthesized in moderate to good yields by the reaction of o-quinone methides photochemically generated from o-(dimethylaminomethyl)phenols with malononitrile. This method was applicable to the synthesis of fluorinated chromenes that were difficult to obtain by other methods. In addition, o-(hydroxymethyl)phenols could be used for the reaction in the presence of tertiary amine bases.
机译:通过从邻-(二甲基氨基甲基)苯酚光化学生成的邻醌甲基化物与丙二腈反应,以中等至良好的产率合成了2-氨基-4H-色烯。该方法适用于其他方法难以获得的氟化二苯甲基的合成。另外,在叔胺碱的存在下,邻-(羟甲基)苯酚可用于反应。

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