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首页> 外文期刊>Letters in organic chemistry >Synthesis of 1,2-Diarylethylenes by Pd-Catalyzed One-Pot Reaction of Benzyl Halides, Tosylhydrazide, and Aryl Aldehydes
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Synthesis of 1,2-Diarylethylenes by Pd-Catalyzed One-Pot Reaction of Benzyl Halides, Tosylhydrazide, and Aryl Aldehydes

机译:通过PD催化的苄卤化物,甲苯肼和芳基醛的PD催化一次性反应合成1,2-二芳基甲苯

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Background: Substituted olefins are versatile functional groups and intermediates in chemistry,medicine, electronics, and optics and materials science fields because of their unique properties.One important class of substituted olefins 1,2-diarylethylenes have attracted considerable attention dueto their presence in both natural products and pharmacologically active substances.Methods: In this paper, we developed a one-pot two-step coupling reaction of aryl aldehydes, tosylhydrazidewith benzyl halides by using inexpensive Pd(PPh3)4 as catalyst, leading to a variety of 1,2-diphenylethenes derivatives with moderate to good yields.Results: The desired 1,2-diarylethylenes were obtained in 46-96% yields via Pd(0)-catalyzed one-potreaction of benzyl halides, tosylhydrazide, and aryl aldehydes.Conclusion: The catalytic system presented here enables the use of easily accessible starting materialsand good functional group tolerance.
机译:背景:取代的烯烃是多功能的官能团和化学,药物和光学和材料科学领域的中间体,因为它们具有独特的特性。重要的烯烃1,2-二芳基乙烯的重要类别引起了相当大的关注Dueto它们在自然中的存在 产品和药理学上活性物质。在本文中,我们通过使用廉价的Pd(PPH3)4作为催化剂,开发了芳基醛,甲苯肼肼苯甲酰卤化物的单步双步偶联反应,导致各种1,2- 二苯基氯替代衍生物,中等至良好的产率。结果:通过Pd(0)在46-96%收率中获得所需的1,2-二芳基乙烯 - 催化苄基卤化物,甲苯肼和芳基醛催化。结论:催化系统 介绍在这里,可以使用易于访问的起始原料和良好的功能组公差。

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