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首页> 外文期刊>Chemistry: A European journal >Highly Convergent Synthesis of Intensively Blue Emissive Furo[2,3-c]isoquinolines by a Palladium-Catalyzed Cyclization Cascade of Unsaturated Ugi Products
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Highly Convergent Synthesis of Intensively Blue Emissive Furo[2,3-c]isoquinolines by a Palladium-Catalyzed Cyclization Cascade of Unsaturated Ugi Products

机译:钯催化的不饱和Ugi产物环化级联反应高强度合成强蓝色发射性呋喃[2,3-c]异喹啉

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摘要

A convergent and diversity-oriented approach to the unusual furo[2,3-c]isoquinoline scaffold is presented. This serendipity-driven approach is characterized by an Ugi multicomponent reaction, which gives the substrate for a palladium-catalyzed insertion-alkynylation-cycloisomerization cascade to provide the furo[2,3-c]isoquinolines in moderate to high yield. Upon UV excitation, all representatives are intensively blue luminescent, as observed by the naked eye, and quantitative fluorescence spectroscopy reveals a considerable effect of the substitution pattern on the quantum yields. The electronic structure is semiquantitatively rationalized by DFT and time-dependent DFT calculations.
机译:提出了一种趋向于多样性的面向非常规呋喃[2,3-c]异喹啉骨架的方法。这种偶然性驱动的方法的特征在于Ugi多组分反应,该反应为钯催化的插入-炔基化-环异构化级联反应提供了底物,从而以中等至高收率提供了呋喃[2,3-c]异喹啉。在紫外激发下,所有代表都是肉眼观察到的强烈蓝色发光,并且定量荧光光谱揭示了取代模式对量子产率的显着影响。电子结构通过DFT和与时间有关的DFT计算进行半定量合理化。

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