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Highly efficient, one-pot synthesis of novel bis-spirooxindoles with skeletal diversity via sequential multi-component reaction in PEG-400 as a biodegradable solvent

机译:通过连续多组分反应在可生物降解溶剂PEG-400中高效地一锅合成具有骨架多样性的新型双螺硫辛多

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摘要

A green and efficient one-pot, sequential, multi-component protocol has been developed for the synthesis of some novel symmetrical bis-spirooxindole derivatives from the reaction of isatins, dihalides, malono derivatives and C–H activated carbonyl compounds or ketene aminal derivatives in the presence of potassium carbonate (K2CO3) in polyethylene glycol 400 (PEG-400) as a biodegradable polymeric solvent at room temperature. In this research, a variety of bis-spiro-indoline-pyranopyranes, bis-spiro-indoline-chromenes, bis-spiro-indoline-pyrido-pyrimidines, bis-spiro-indoline-imidazo-pyridines and bis-spiro-indoline-pyridines were obtained with excellent yields within short reaction time and without chromatographic separation.
机译:已开发出一种绿色高效的一锅,顺序,多组分方案,该方案用于从靛红,二卤化物,丙二酸衍生物和CH活化的羰基化合物或乙烯酮缩醛衍生物反应中合成一些新颖的对称双螺氧并吲哚衍生物。聚乙二醇400(PEG-400)中碳酸钾(K 2 CO 3 )的存在在室温下可生物降解的聚合物溶剂。在这项研究中,各种双-螺-吲哚-吡喃并吡喃,双-螺-吲哚并-色胺,双-螺-吲哚并-吡啶-嘧啶,双-螺-吲哚并-咪唑并吡啶和双-螺-吲哚并吡啶在短反应时间内以优异的收率获得了目标化合物,无需色谱分离。

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