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手性醛-钯催化通过级联 Heck-烷基化反应实现α-烷基色氨酸的不对称合成。

Chiral Aldehyde-Palladium Catalysis Enables Asymmetric Synthesis of α-Alkyl Tryptophans via Cascade Heck-Alkylation Reaction.

机构信息

Key Laboratory of Applied Chemistry of Chongqing Municipality, School of Chemistry and Chemical Engineering, Southwest University, Chongqing, 400715, China.

出版信息

Org Lett. 2023 May 5;25(17):3163-3167. doi: 10.1021/acs.orglett.3c01119. Epub 2023 Apr 25.

Abstract

The first catalytic asymmetric cascade Heck-alkylation reaction of NH-unprotected amino acid esters with -(2-iodophenyl)allenamides is reported in this work. Under the promotion of a combining catalytic system comprising a chiral aldehyde, a chiral palladium complex, and the Lewis acid ZnCl, the title reaction takes place smoothly, giving optically active α-alkyl tryptophan derivatives in moderate to good yields and excellent enantioselectivities. The target products can be converted into other structurally complex chiral indoles without the loss of enantioselectivities.

摘要

本文报道了首例 NH 未保护的氨基酸酯与 -(2-碘代苯)烯丙酰胺的不对称催化串联 Heck-烷基化反应。在包含手性醛、手性钯配合物和路易斯酸 ZnCl 的组合催化体系的促进下,标题反应顺利进行,以中等至良好的收率和优异的对映选择性得到了光学活性的α-烷基色氨酸衍生物。目标产物可以在不损失对映选择性的情况下转化为其他结构复杂的手性吲哚。

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