首页> 外文期刊>RSC Advances >Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines
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Spiro-condensation of 5-methoxycarbonyl-1H-pyrrole-2,3-diones with cyclic enoles to form spiro substituted furo[3,2-c]-coumarins and quinolines

机译:用循环雌激素螺旋氧化5-甲氧基羰基-1H-吡咯-2,3-致浓缩的螺旋溶解,形成螺旋取代呋喃[3,2-C] -coumarins和喹啉

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摘要

Highly efficient spiro-condensation enabling cyclic enoles to act as 1,3-bis-nucleophiles in reaction with pyrrole-2,3-diones acting as 1,2-bis-electrophiles was developed. The corresponding furo[3,2- c ]coumarins and furo[3,2- c ]quinolines containing a spiro pyrrole fragment were obtained in high yields.
机译:开发了高效的螺凝固,使循环溶解充当1,3-双亲核试剂与吡咯-2,3-致力作用作为1,2-BIS-Methicophers的反应。相应的呋喃[3,2-c]香豆素和含有螺吡咯片段的含有高产率的呋喃[3,2- C]喹啉。

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