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Ring-closure Reaction to Novel Quinoline Derivatives and Their Structural Characterization
作者姓名:吕银祥  蓝碧健  周辉  徐伟  王静梅  黄永明
作者单位:[1]DepartmentofMaterialsScience,FudanUniversity,Shanghai200433,China [2]DepartmentofChemistry,FudanUniversity,Shanghai200433,China [3]ResearchCenterforAnalysisandMeasurment,FudanUniversity,Shanghai200433,China
基金项目:Project supported by the National Natural Science Foundation of China (No. 60171008) and the Ministry of Education,China.
摘    要:In the condensation of arylaldehydes with arylethylidenemalononitriles, it was found that, besides the normal product dienes a, the ring-closure product quinoline derivatives b can be also obtained in 26%--50% yields. The substituent effects were also examined and a possible reaction mechanism was proposed for the formation of b. The X-ray crystal structure of lb confirms the structure of the ring-closure product.

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Ring-closure Reaction to Novel Quinoline Derivatives and Their Structural Characterization
Yin‐Xiang Lu,Bi‐Jian Lan,Hui Zhou,Wei Xu,Jing‐Mei Wang,Yong‐Ming Huang.Ring-closure Reaction to Novel Quinoline Derivatives and Their Structural Characterization[J].Chinese Journal of Chemistry,2004,22(8):854-858.
Authors:Yin‐Xiang Lu  Bi‐Jian Lan  Hui Zhou  Wei Xu  Jing‐Mei Wang  Yong‐Ming Huang
Abstract:In the condensation of arylaldehydes with arylethylidenemalononitriles, it was found that, besides the normal product dienes a, the ring‐closure product quinoline derivatives b can be also obtained in 26%–50% yields. The substituent effects were also examined and a possible reaction mechanism was proposed for the formation of b. The X‐ray crystal structure of 1b confirms the structure of the ring‐closure product.
Keywords:arylaldehyde  arylethylidenemalononitrile  ring closure  X-ray diffraction
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