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首页> 外文期刊>Organic letters >High-pressure accelerated asymmetric organocatalytic friedel-crafts alkylation of indoles with enones: Application to quaternary stereogenic centers construction
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High-pressure accelerated asymmetric organocatalytic friedel-crafts alkylation of indoles with enones: Application to quaternary stereogenic centers construction

机译:带有烯酮的吲哚的高压加速不对称有机催化弗瑞德-克分子烷基化:在四元立体异构中心建设中的应用

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摘要

An organocatalytic Friedel-Crafts alkylation of indoles with α,β-unsaturated ketones was found to be efficiently accelerated under high-pressure conditions with a low loading of chiral primary amine salts with good yield and enantioselectivity up to 90%. This approach also allows, for the first time, selected indole derivatives containing quaternary stereogenic centers to be obtained from prochiral β,β-disubstituted enones with an enantioselectivity up to 80%.
机译:发现具有α,β-不饱和酮的吲哚的有机催化的吲哚的弗里德-克来福特烷基化在高压条件下以低负载量的手性伯胺盐的负载可有效地加速,产率高,对映选择性高达90%。该方法还首次允许从前手性β,β-二取代的烯酮中获得对映体选择性高达80%的选定的含有季立体异构中心的吲哚衍生物。

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