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首页> 外文期刊>Chemistry - A European Journal >Asymmetric Conjugate Addition of Nitromethane to Enones Catalyzed by Chiral N,N′-Dioxide–Scandium(III) Complexes
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Asymmetric Conjugate Addition of Nitromethane to Enones Catalyzed by Chiral N,N′-Dioxide–Scandium(III) Complexes

机译:N,N'-二氧化物-Scan(III)配合物催化硝基甲烷与烯酮的不对称共轭加成反应

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摘要

Chalk it up as a “Sc”andal: The asymmetric conjugate addition of chalcone and “cinnamone” derivatives to nitromethane has been realized by using a simple and efficient scandium(III)–N,N′-dioxide complex as the catalyst (see scheme). In the presence of 2–5 mol % catalyst loading, the corresponding products were formed in excellent yields (up to 99 %) and enantioselectivities (up to99 % ee).
机译:以“ Sc”形式存在:通过简单有效的scan(III)-N,N'-二氧化物络合物作为催化剂,实现了查尔酮和“肉桂酮”衍生物向硝基甲烷的不对称共轭加成反应(见方案) )。在2-5 loadingmol%的催化剂负载量下,形成的相应产物的收率(高达99%)和对映选择性(高达> 99%ee)都很高。

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