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首页> 外文期刊>Chemistry: A European journal >Catalytic asymmetric direct vinylogous michael addition of deconjugated butenolides to maleimides for the construction of quaternary stereogenic centers
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Catalytic asymmetric direct vinylogous michael addition of deconjugated butenolides to maleimides for the construction of quaternary stereogenic centers

机译:催化不对称直接乙烯基共价键将解偶联的丁烯内酯添加到马来酰亚胺中,用于构建四元立体异构中心

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摘要

Competition under control: A practical and efficient direct asymmetric vinylogous Michael reaction of deconjugated butenolides has been developed (see scheme). The products of this reaction, highly functionalized chiral succinimides, are obtained in excellent yield with high diastereoselectivity (up to d.r.=18:1) and outstanding enantioselectivity (up to e.r.=99.5:0.5).
机译:竞争得到控制:已开发了实用,有效的解偶联丁烯内酯直接不对称乙烯基迈克尔反应(请参阅方案)。该反应的产物,高度官能化的手性琥珀酰亚胺,以优异的产率获得,具有高的非对映选择性(高达d.r. = 18∶1)和出色的对映选择性(高达e.r. = 99.5∶0.5)。

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