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1,5-二氮杂双环[4,3,0]壬碳-5-烯与全氟炔酸酯的反应及其产物的核磁共振研究
引用本文:施志坚,聂玲清,曹卫国.1,5-二氮杂双环[4,3,0]壬碳-5-烯与全氟炔酸酯的反应及其产物的核磁共振研究[J].分析化学,2003,31(5):573-576.
作者姓名:施志坚  聂玲清  曹卫国
作者单位:上海大学化学系,上海,200436
基金项目:国家自然科学基金资助项目(No.20172037)
摘    要:1,5—二氮杂双环4,3,0]壬碳—5—烯(DBN)与全氟炔酸酯反应生成成环化合物。通过对成环产物的^1HNMR、^13C NMR及相关的2D NMR谱的分析,确证了该类化合物的结构,并讨论了其化学位移及J-偶合特征。同时提出了整个反应可能的历程和机理。

关 键 词:1,5-二氮杂双环[4,3,0]壬碳-5-烯  全氟炔酸酯  产物  核磁共振  化学反应  迈克尔加成反应  结构

Reaction of 1,5-Diazabicyclo[4,3,0]non-5-ene and Perfluoroalkynoates and Study on the Nuclear Magnetic Resonance Spectra of the Products
Shi Zhijian,Nie Lingqing,Cao Weiguo.Reaction of 1,5-Diazabicyclo[4,3,0]non-5-ene and Perfluoroalkynoates and Study on the Nuclear Magnetic Resonance Spectra of the Products[J].Chinese Journal of Analytical Chemistry,2003,31(5):573-576.
Authors:Shi Zhijian  Nie Lingqing  Cao Weiguo
Abstract:The tricyclic derivative was formed by the reaction of 1 ,5-diazabicyclo4,3,0] non -5-ene (DBN) and perfluoro-2-alkynoates. The products were analyzed in detail by 1H nuclear magnetic resonance (NMR),13C NMR and 2D NMR. Their chemical shifts and /-coupling constants were discussed. The reaction paths and mechanism were also proposed.
Keywords:Nuclear magnetic resonance  1  5-diazabicyclo[4  3  0]non-5-ene  perfluoroalkynoates
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