首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Highly effective and enantioselective Michael addition of 4-hydroxycoumarin to α,β-unsaturated ketones promoted by simple chiral primary amine thiourea bifunctional catalysts
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Highly effective and enantioselective Michael addition of 4-hydroxycoumarin to α,β-unsaturated ketones promoted by simple chiral primary amine thiourea bifunctional catalysts

机译:简单手性伯胺硫脲双功能催化剂促进α-β-不饱和酮与4-羟基香豆素的高效对映选择性迈克尔加成反应

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摘要

Highly asymmetric Michael addition of 4-hydroxycoumarin to α,β-unsaturated ketones promoted by chiral primary amine thiourea bifunctional catalysts was developed and a series of Michael adducts were obtained in excellent yields (up to 97%) and enantioselectivities (up to 95% ee). Optically pure S-warfarin was easily obtained in 99% ee after single recrystallization.
机译:开发了4-羟基香豆素向手性伯胺硫脲双功能催化剂促进的α,β-不饱和酮上的高度不对称迈克尔加成反应,并获得了一系列迈克尔加合物,收率极高(高达97%)和对映选择性(高达95%ee) )。一次重结晶后,很容易在99%ee中获得光学纯的S-华法林。

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