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首页> 外文期刊>Bulletin of the Korean Chemical Society >Enantioselective Electrophilic α-Amination of α-Cyanoketones Catalyzed by Chiral Nickel Complexes
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Enantioselective Electrophilic α-Amination of α-Cyanoketones Catalyzed by Chiral Nickel Complexes

机译:手性镍配合物催化α-氰基酮的对映选择性亲电子α-氨基化

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摘要

The efficient synthetic construction of α-amino carbonyl compounds is one of the most intensely studied areas in organic synthesis. Chiral α-amino nitriles are very useful bifunctional compounds for a large number of synthetic applications. The most popular and wide use of chiral α-amino nitrile involves hydrolysis of the nitrile group to generate chiral α-amino acids which are often used as key building blocks in pharmaceuticals. In addition, since cyano group is easily converted to other functional groups, chiral α-substiruted α-amino nitriles would be versatile synthetic intermediates for the synthesis of chiral 1,2-diamine derivatives which are employed as medicinal agents or chiral ligands.
机译:α-氨基羰基化合物的有效合成结构是有机合成中研究最深入的领域之一。手性α-氨基腈是用于大量合成应用的非常有用的双官能化合物。手性α-氨基腈的最流行和广泛使用涉及腈基的水解以产生手性α-氨基酸,其通常用作药物中的关键组成部分。另外,由于氰基易于转化为其他官能团,手性α-取代的α-氨基腈将是用于合成用作药物或手性配体的手性1,2-二胺衍生物的通用合成中间体。

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