通过 CN 偶联和多组分自由基/极性交叉光氧催化烯烃的双官能化

IF 1.5 4区 化学 Q3 CHEMISTRY, ORGANIC Tetrahedron Letters Pub Date : 2024-08-14 DOI:10.1016/j.tetlet.2024.155223
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引用次数: 0

摘要

我们报告了一种烷基噻蒽盐类(TTs)参与的三组分自由基烯烃双官能化反应。通过这种温和的方法实现了苯胺的烷基化。该策略可能涉及氧化自由基/极性交叉,实现了极性化学和自由基化学的结合。各种苯胺、伯烷基取代 TTs、仲烷基取代 TTs 和烯烃都能以中等至良好的收率获得。我们的工作为生产各种官能化苯胺衍生物提供了宝贵的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Photoredox-catalyzed difunctionalization of alkenes through CN coupling and multicomponent radical/polar crossover

We reported an alkyl-thianthrenium salts (TTs) involved three-component radical alkene difunctionalization reaction. Alkylation of anilines has been realized via this mild method. An oxidative radical/polar crossover may be involved in the strategy, which realizing the combination of polar chemistry and radical chemistry. A variety of anilines, primary alkyl-substituted TTs, secondary alkyl-substituted TTs and olefins could be accessed in medium to good yield. Our work provides a valuable approach to producing diverse functionalized aniline derivatives.

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来源期刊
Tetrahedron Letters
Tetrahedron Letters 化学-有机化学
CiteScore
3.50
自引率
5.60%
发文量
521
审稿时长
28 days
期刊介绍: Tetrahedron Letters provides maximum dissemination of outstanding developments in organic chemistry. The journal is published weekly and covers developments in techniques, structures, methods and conclusions in experimental and theoretical organic chemistry. Rapid publication of timely and significant research results enables researchers from all over the world to transmit quickly their new contributions to large, international audiences.
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