Ring-closure Reaction to Novel Quinoline Derivatives and Their Structural Characterization  

Ring-closure Reaction to Novel Quinoline Derivatives and Their Structural Characterization

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作  者:吕银祥 蓝碧健 周辉 徐伟 王静梅 黄永明 

机构地区:[1]Department of Materials Science, Fudan University, Shanghai 200433, China [2]Department of Materials Science, Fudan University Shanghai 200433, China [3]Department of Chemistry, Fudan University, Shanghai 200433, China [4]Research Center for Analysis and Measurment, Fudan University, Shanghai 200433, China

出  处:《Chinese Journal of Chemistry》2004年第8期854-858,共5页中国化学(英文版)

基  金: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 1b confirms the structure of the ring-closure product.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.

关 键 词:ARYLALDEHYDE arylethylidenemalononitrile ring closure X-ray diffraction 

分 类 号:O621.25[理学—有机化学]

 

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