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首页> 外文期刊>Bulletin of the Korean Chemical Society >Synthesis of 2-Benzylidene-7a-alkyltetrahydropyrrolizine-3,5-diones Starting from Baylis-Hillman Adducts
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Synthesis of 2-Benzylidene-7a-alkyltetrahydropyrrolizine-3,5-diones Starting from Baylis-Hillman Adducts

机译:从Baylis-Hillman加合物开始合成2-苄基-7a-烷基四氢吡咯烷嗪-3,5-二酮

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摘要

Recently,3-alkylidenedihydropyrrol-2-ones~(1a)and 3-alkyl-idenedihydropyrrole derivatives were synthesized starting from the Baylis-Hillman adducts of methyl acrylate and methyl vinyl ketone,respectively.These compounds were prepared by the reductive cyclization of nitroalkane derivatives,which were synthesized from the Baylis-Hillman acetate by the S_N2' reaction with primary nitroalkane,as shown in Scheme 1.
机译:近年来,分别从丙烯酸甲酯和甲基乙烯基酮的Baylis-Hillman加合物开始合成3-亚烷基二氢吡咯-2-酮〜(1a)和3-烷基二氢吡咯衍生物。这些化合物是通过硝基烷衍生物的还原环化反应制备的。如方案1所示,它们是通过Bayes-Hillman乙酸酯通过S_N2'与伯硝基烷的反应合成的。

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