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由硫叶立德、亚硝基芳烃和炔烃合成二酮氮丙啶和高官能化烯烃的三组分反应

Three-Component Synthesis of Di-Keto Aziridines and Highly Functionalized Alkenes from Sulfoxonium Ylides, Nitrosoarenes, and Alkynes.

作者信息

Zhai Pingan, Fang Yongsheng, Li Wenhui, Lin Jianying, Li Xing

机构信息

College of Biomedical Engineering, Taiyuan University of Technology, 79 West Yingze Street, Taiyuan 030024, People's Republic of China.

出版信息

J Org Chem. 2023 Sep 1;88(17):12194-12207. doi: 10.1021/acs.joc.3c00062. Epub 2023 Aug 17.

Abstract

A catalyst-free one-pot three-component method of sulfoxonium ylides, nitrosoarenes, and alkynes for the synthesis of highly functionalized di-keto aziridines and alkenes is described. This strategy features the catalyst-free and additive-free approach, the employment of safe, more stable, and readily accessible sulfoxonium ylides, which bear a much wider substrate scope as starting materials. In terms of terminal alkynes, a cascade reaction of nitrone formation/1,3-diploar cycloaddition/Baldwin rearrangement is involved to afford a wide variety of di-keto aziridines. However, highly functionalized alkenes could be obtained instead of di-keto aziridines through the same nitrone formation/1,3-diploar cycloaddition and another different rearrangement reaction when internal alkynes are employed as starting materials.

摘要

描述了一种用于合成高度官能化二酮氮丙啶和烯烃的无催化剂一锅三组分方法,该方法使用了锍叶立德、亚硝基芳烃和炔烃。此策略具有无催化剂和无添加剂的特点,采用了安全、更稳定且易于获得的锍叶立德作为起始原料,其底物范围更广。对于末端炔烃,涉及硝酮形成/1,3-偶极环加成/鲍德温重排的串联反应,以提供多种二酮氮丙啶。然而,当使用内炔烃作为起始原料时,通过相同的硝酮形成/1,3-偶极环加成和另一种不同的重排反应,可以得到高度官能化的烯烃而非二酮氮丙啶。

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