首页> 外文期刊>Journal of combinatorial chemistry >Application of β-(2-Chloroaroyl)thioacetanilide in Synthesis(III): An Efficient Three-Component Synthesis of Thiochromeno[2,3-b]pyridines Catalyzed by KF/Neutral A12O3 Co-operated with PEG 6000 under Microwave Irradiation
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Application of β-(2-Chloroaroyl)thioacetanilide in Synthesis(III): An Efficient Three-Component Synthesis of Thiochromeno[2,3-b]pyridines Catalyzed by KF/Neutral A12O3 Co-operated with PEG 6000 under Microwave Irradiation

机译:β-(2-氯代芳酰基)硫代乙酰胺在合成(III)中的应用:微波辐射下KF /中性Al2O3与PEG 6000协同催化高效合成三硫代噻吩并[2,3-b]吡啶

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摘要

A series of new functionalized thiochromeno[2,3-b]pyridine derivatives have been synthesized via a sequence of Knoevenagel condensation, Michael addition, cyclization, and intramolecular nucleophilic substitution, which is first catalyzed by KFeutral A12O3 cooperated with PEG 6000 under microwave irradiation. Experimental results indicated that among the catalysts tested, KF/ neutral A12O3 with PEG 6000 exhibits the best catalytic activity, which leads to a substantial improvement in the overall yield and purity of the desired final products and significantly shorter reaction time.
机译:通过Knoevenagel缩合,Michael加成,环化和分子内亲核取代的一系列合成了一系列新的功能化的硫代色素[2,3-b]吡啶衍生物,首先由KF /中性A12O3与PEG 6000协同微波催化辐射。实验结果表明,在所测试的催化剂中,具有PEG 6000的KF /中性Al2O3表现出最佳的催化活性,从而导致所需最终产品的总收率和纯度得到显着提高,并且反应时间明显缩短。

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