首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Ultrasound Assisted Pictet-Spengler Synthesis of Tetrahydro--Carboline Derivatives
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Ultrasound Assisted Pictet-Spengler Synthesis of Tetrahydro--Carboline Derivatives

机译:超声辅助Pictet-Spengler合成四氢-咔啉衍生物

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摘要

The synthesis of twelve tetrahydro--carboline derivatives 3a, 3b, 3c, 3d, 3e, 3f, 3g, 3h, 3i, 3j, 3k, 3l prepared via the Pictet-Spengler reaction is described. The reaction of tryptamine and a variety of arylaldehydes were carried out under ultrasonic irradiation and trifluoracetic acid catalysis at room temperature. These tetrahydro--carbolines have been synthesized in higher yields and shorter reaction times compared to the conventional method. Moreover, the reaction proceeded successfully even employing arylaldehydes with electron-donating or electron-attracting substituents which did not react under conventional method.
机译:描述了通过Pictet-Spengler反应制备的十二种四氢咔啉衍生物3a,3b,3c,3d,3e,3f,3g,3h,3i,3j,3k,3l的合成。在室温下,在超声辐射和三氟乙酸催化下,进行了色胺与多种芳基醛的反应。与常规方法相比,这些四氢咔啉的合成产率更高,反应时间更短。而且,即使使用带有给电子或吸引电子的取代基的芳醛也能成功地进行反应,而该给电子或吸电子的取代基在常规方法下不会发生反应。

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