几种N-取代马来酰胺酸辅酶模型的核磁共振研究  

~1H NMR, ^(13)C NMR STUDY OF 8 N-ARYL MALEINAMIC ACIDS

作　　者：颜叙秀[1] 胡玉仙[1] 陈亮[2] 

机构地区：[1]山西大学分子所 [2]山西大学分析测试中心,太原030006

出　　处：《波谱学杂志》2002年第1期63-67,共5页Chinese Journal of Magnetic Resonance

基　　金：山西省归国人员基金资助项目

摘　　要：我们对８种Ｎ－取代马来酰胺酸辅酶模型与不同类型的亲核试剂反应后生成的产物进行了１Ｈ、１３Ｃ ＮＭＲ的研究，测得１Ｈ、１３Ｃ谱化学位移，研究探讨其规律性，并测试了ＩＲ谱和元素分析．The 1H NMR 13C NMR spectra of 8 N-Aryl maleinamic acids coenzyme mockup with the productes reacted variant kind of nucleophiles were studied. The 1H and 13C chemi- cal shifts were obtained and their regularity has been researched. Their elemental analysis and JR spectra have been characterized. The reaction products of eight N-aryl maleinamic acids coenzyme mockup with various kinds of nucleophiles were studied by 1H and 13C NMR spectroscpy.

关 键 词：马来酰胺酸 辅酶 ^1HNMR ^13CNMR 模型 核磁共振分析 结构特征 仿生化学 

分 类 号：Q552[生物学—生物化学] O6－05[理学—化学]