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Copper-promoted cross-coupling of nitroarenes with 4-alkyl-1,4-dihydropyridines using a peroxide-driven radical reductive strategy
Organic Chemistry Frontiers ( IF 5.4 ) Pub Date : 2022-06-17 , DOI: 10.1039/d2qo00706a
Hui-Min Jiang 1 , Jing-Hao Qin 1 , Qing Sun 1 , Dong Zhang 1 , Jin-Peng Jiang 1 , Xuan-Hui Ouyang 1 , Ren-Jie Song 1 , Jin-Heng Li 1, 2, 3
Affiliation  

A copper-promoted reductive cross-coupling of nitroarenes with 4-alkyl-1,4-dihydropyridines for producing N-alkylbenzenamines is described. Using 4-alkyl-1,4-dihydropyridines as alkyl radical sources and internal reducing agents enables the construction of C(sp3)–N bonds under oxidative conditions, which provide an elegant complementary platform to assemble N-alkylbenzenamines with good tolerance for sensitive functional groups.

中文翻译:

使用过氧化物驱动的自由基还原策略铜促进硝基芳烃与 4-烷基-1,4-二氢吡啶的交叉偶联

描述了一种铜促进的硝基芳烃与 4-烷基-1,4-二氢吡啶的还原交叉偶联,用于生产N-烷基苯胺。使用 4-烷基-1,4-二氢吡啶作为烷基自由基源和内部还原剂能够在氧化条件下构建 C(sp 3 )-N 键,这为组装N-烷基苯胺提供了一个优雅的互补平台,对敏感物质具有良好的耐受性官能团。
更新日期:2022-06-17
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