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首页> 外文期刊>Organic letters >Catalytic Asymmetric Formal Insertion of Aryldiazoalkanes into the C-H Bond of Aldehydes: Synthesis of Enantioenriched Acyclic alpha-Tertiary Aryl Ketones
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Catalytic Asymmetric Formal Insertion of Aryldiazoalkanes into the C-H Bond of Aldehydes: Synthesis of Enantioenriched Acyclic alpha-Tertiary Aryl Ketones

机译:芳基重氮烷烃催化不对称形式插入醛的C-H键:富含对映体的无环α-叔芳基酮的合成

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摘要

A novel, catalytic enantioselective route to synthesize a variety of a-tertiary aryl ketones via a boron Lewis acid promoted formal insertion of aryldiazoalkane into the C-H bond of both aromatic and aliphatic aldehydes is described. In the presence of chiral (S)-oxazaborolidinium ion catalyst 1, the reaction proceeded in good yields (up to 94%) with excellent enantioselectivities (up to 99% ee).
机译:描述了一种新颖的催化对映选择性路线,该路线通过硼路易斯酸促进芳基重氮烷烃正式插入芳族和脂族醛的C-H键中来合成各种α-叔芳基酮。在手性(S)-恶唑硼烷鎓离子催化剂1的存在下,反应以良好的收率(最高94%)和优异的对映选择性(最高99%ee)进行。

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