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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 >Synthesis of methyl substituted [5,6]- and [7,8]-fused pyridocoumarins via the iodine-catalyzed reaction of aminocoumarins with n-butyl vinyl ether
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Synthesis of methyl substituted [5,6]- and [7,8]-fused pyridocoumarins via the iodine-catalyzed reaction of aminocoumarins with n-butyl vinyl ether

机译:通过氨基香豆素与正丁基乙烯基醚的碘催化反应合成甲基取代的[5,6]-和[7,8]-融合的吡啶香豆素

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摘要

2-Methyl substituted [5,6]- or [7,8]-fused pyridocoumarins are prepared from the Povarov-type, three-component reactions of 6- or 7-aminocoumarins with n-butyl vinyl ether, catalyzed by iodine in refluxing acetonitrile, through the aza-Diels-Alder reaction of the initially formed N-iminoaminocoumarins with a second equivalent of the vinyl ether.
机译:2-甲基取代的[5,6]-或[7,8]-融合吡啶并香豆素是由碘催化的6-或7-氨基香豆素与正丁基乙烯基醚的Povarov型三组分反应制备的乙腈,通过最初形成的N-亚氨基氨基香豆素与第二当量的乙烯基醚的aza-Diels-Alder反应。

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