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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 >Highly enantioselective Michael addition of alpha,alpha-disubstituted aldehydes to maleimides catalyzed by new primary amine-squaramide bifunctional organocatalysts
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Highly enantioselective Michael addition of alpha,alpha-disubstituted aldehydes to maleimides catalyzed by new primary amine-squaramide bifunctional organocatalysts

机译:高映选择性迈克尔加入α-二取代的醛与新的伯胺 - 鳞甲酰胺双官能有机催化剂催化的马来酰亚胺

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摘要

New bifunctional primary amine-squaramides catalyzed asymmetric Michael addition reaction of alpha,alpha-disubstituted aldehydes to maleimides has been developed. This organocatalytic asymmetric reaction provides easy access to functionalized succinimides with a broad substrate scope. Both enantiomers of desired succinimide derivatives were obtained in good to excellent yields (up to 98%) with excellent enantioselectivities (up to >99% ee). (C) 2017 Elsevier Ltd. All rights reserved.
机译:已经开发出催化非对称初级胺 - 氨基催化α的非对称迈克尔加成反应,已经开发了对马来酰亚胺的α-二取代的醛。 该有机催化不对称反应提供易于获得具有宽基底范围的官方琥珀酰亚胺。 优异的琥珀酰亚胺衍生物的对映异构体良好地获得优异的产率(高达98%),具有优异的对映射性(高达> 99%EE)。 (c)2017 Elsevier Ltd.保留所有权利。

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