首页> 外文期刊>Chemical science >Enantioselective construction of C-chiral allylic sulfilimines via the iridium-catalyzed allylic amination with S,S-diphenylsulfilimine: asymmetric synthesis of primary allylic amines
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Enantioselective construction of C-chiral allylic sulfilimines via the iridium-catalyzed allylic amination with S,S-diphenylsulfilimine: asymmetric synthesis of primary allylic amines

机译:通过 S S -二苯硫亚胺的铱催化的烯丙基胺化对 C -手性烯丙基硫亚胺的对映选择性:伯烯丙基胺的不对称合成

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We have devised a highly regio- and enantioselective iridium-catalyzed allylic amination reaction with the sulfur-stabilized aza-ylide, S,S-diphenylsulfilimine. This process provides a robust and scalable method for the construction of aryl-, alkyl- and alkenyl-substituted C-chiral allylic sulfilimines, which are important functional groups for organic synthesis. Additionally, the combination of the allylic amination with an in situ deprotection of the sulfilimine constitutes a convenient one-pot protocol for the construction of chiral nonracemic primary allylic amines.
机译:我们设计了一种具有高区域和对映选择性的铱催化的烯丙基胺化反应,该反应与硫稳定的氮杂内酯 S S -二苯基硫亚胺形成。该方法为构建芳基,烷基和烯基取代的 C -手性烯丙基亚硫亚胺提供了鲁棒且可扩展的方法,这是有机合成的重要官能团。另外,烯丙基胺化与亚硫亚胺的就地脱保护的组合构成了用于构建手性非外消旋伯烯丙基胺的方便的一锅法方案。

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