NiCl2Py2/IMes - HCl/ButONa 系统催化的唑与烯的烷基化反应

IF 1.7 4区 化学 Q3 CHEMISTRY, MULTIDISCIPLINARY Russian Chemical Bulletin Pub Date : 2024-10-26 DOI:10.1007/s11172-024-4380-x
O. V. Khazipov, V. M. Chernyshev
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引用次数: 0

摘要

在 N-杂环碳镍络合物(Ni/NHC)的催化下,开发出了一种唑与烯烃烷基化的新方法。具有催化活性的 Ni/NHC 复合物是由空气稳定的前体原位形成的:与吡啶的氯化镍复合物 (NiCl2Py2)、作为碳源的咪唑盐 IMes-HCl(IMes 是 1,3-双(2,4,6-三甲基苯基)-1,3-二氢-2H-咪唑-2-亚基)和叔丁醇钠 (ButONa)。所开发方法的优点是催化系统的各种成分均可获得,无需使用特殊制剂将 NiII 还原成 Ni0,而且简化了合成过程。
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Alkylation of azoles with alkenes catalyzed by the NiCl2Py2/IMes • HCl/ButONa system

A new approach to the alkylation of azoles with alkenes catalyzed by the nickel complexes with N-heterocyclic carbenes (Ni/NHC) was developed. The catalytically active Ni/NHC complexes are formed in situ from the air-stable precursors: the nickel chloride complex with pyridine (NiCl2Py2), imidazolium salt IMes•HCl (IMes is 1,3-bis(2,4,6-trimethylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene) as the carbene source, and sodium tert-butoxide (ButONa). The advantages of the developed approach are availability of the components of the catalytic system, no necessity to apply special agents for the reduction of NiII to Ni0, and simplification of the synthesis procedure.

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来源期刊
Russian Chemical Bulletin
Russian Chemical Bulletin 化学-化学综合
CiteScore
2.70
自引率
47.10%
发文量
257
审稿时长
3-8 weeks
期刊介绍: Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections: General and Inorganic Chemistry; Physical Chemistry; Organic Chemistry; Organometallic Chemistry; Chemistry of Natural Compounds and Bioorganic Chemistry.
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