基于α-酮酰胺合成的新方法学分析-new methodological analysis based on synthesis of α -ketoamide.docxVIP

目录第一章 背景介绍 ................................................................................................ 11.1 引言 ............................................................................................................... 11.2 关于酮酰胺的研究现状................................................................................. 21.3 参考文献........................................................................................................ 5第二章 苯乙酮与二级胺的氧化偶联反应 ................................................... 8 2.1 研究背景........................................................................................................ 82.2 无金属条件下苯乙酮和二级胺的氧化偶联反应..........................................132.3 实验部分.......................................................................................................192.4 参考文献.......................................................................................................25第三章 1,3-二酮通过 C–C 键断裂与二级胺氧化偶联反应293.1 研究背景.......................................................................................................293.2 无金属条件下 1,3-二酮与二级胺的氧化偶联反应 .....................................333.3 实验部分.......................................................................................................403.4 参考文献.......................................................................................................47第四章 三级胺通过 C–N 键断裂与酮酸的胺化反应504.1 研究背景.......................................................................................................504.2 银催化的三级胺与?–酮酸的胺化反应 ........................................................534.3 实验部分.......................................................................................................584.4 参考文献.......................................................................................................66附录Ⅰ部分化合物的谱图 ...............................................................................69附录Ⅱ硕士期间发表论文题录 ......................................................................83致谢.............