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A simple primary amine thiourea catalyzed highly enantioselective conjugate addition of α,α-disubStituted aldehydes to maleimides

机译:简单的伯胺硫脲催化α,α-二取代醛向马来酰亚胺的高对映选择性共轭加成

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摘要

(Figure Presented) Branch point: A simple primary amine thiourea catalyzed highly enantioselective conjugate addition of α,α-disubstituted aldehydes to maleimides has been developed. The biologically useful chiral disubstituted α-branched succinimides are attained with the generation of two contiguous quaternary and/or tertiary stereogenic centers in one step with excellent enantioselectivities and in high yields under mild reaction conditions (see scheme).
机译:(显示的图)分支点:已经开发了一种简单的伯胺硫脲催化的α,α-二取代醛向马来酰亚胺的高对映选择性共轭加成反应。具有生物学上有用的手性二取代的α-支化琥珀酰亚胺是通过在温和的反应条件下,以极好的对映选择性和高收率一步生成两个连续的季和/或叔立体异构中心而获得的(参见方案)。

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