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首页> 外文期刊>Advanced synthesis & catalysis >Direct Synthesis of 4-Organylselanylpyrazoles by Copper-Catalyzed One-Pot Cyclocondensation and C-H Bond Selenylation Reactions
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Direct Synthesis of 4-Organylselanylpyrazoles by Copper-Catalyzed One-Pot Cyclocondensation and C-H Bond Selenylation Reactions

机译:铜催化一锅环缩合反应和C-H键硒化反应直接合成4-有机基硒基吡唑

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摘要

We describe herein an efficient protocol to synthesize selanyl-substituted pyrazoles by cyclocondensation and copper-catalyzed direct C-H bond selenation reactions. The products were obtained in moderate to excellent yields by the onepot multicomponent reactions of hydrazines, 1,3-diketones and diorganyl diselenides, using catalytic amounts of copper bromide and bipyridine. These reactions tolerated a range of substituents in the starting materials and proved to be an efficient methodology for combinatorial synthesis of new selenium-containing pyrazoles with potential applications in biological studies.
机译:我们在本文中描述了一种有效的方案,其通过环缩合和铜催化的直接C-H键硒化反应来合成硒基取代的吡唑。通过使用催化量的溴化铜和联吡啶,通过肼,1,3-二酮和二有机基二硒化物的一锅多组分反应,以中等至优异的产率获得了产物。这些反应可耐受起始材料中的一系列取代基,并被证明是组合合成新的含硒吡唑的有效方法,在生物学研究中具有潜在的应用。

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