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机构地区:[1]Department of Chemistry, University of Science and Technology of China, Hefei, Anhui 230026, China [2]College of Chemistry, Lanzhou University, Lanzhou, Gansu 730000, China
出 处:《Chinese Journal of Chemistry》2007年第1期95-97,共3页中国化学(英文版)
基 金:Project supported by the National Natural Science Foundation of China (No. 20072036) and the Specialized Research Fund for the Doctoral Program of Higher Education of China.
摘 要:The reaction of a series of 1-(3-pyridyl)-2,2-di-substituted ethylenes with 1-benzyl-1,4-dihydronicotinamide (BNAH) in deaerated acetonitrile produces the corresponding 1-(3-pyridyl)-2,2-di-substituted ethanes in contrast to benzylidenemalononitrile (BM) which does not react with BNAH under the same conditions.The reaction of a series of 1-(3-pyridyl)-2,2-di-substituted ethylenes with 1-benzyl-1,4-dihydronicotinamide (BNAH) in deaerated acetonitrile produces the corresponding 1-(3-pyridyl)-2,2-di-substituted ethanes in contrast to benzylidenemalononitrile (BM) which does not react with BNAH under the same conditions.
关 键 词:1-benzyl-1 4-dihydronicotinamide 1-(3-pyridyl)-2 2-di-substituted ethylene benzylidenemalononitrile concerted hydride transfer
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