红紫素-18二酰亚胺的化学反应及其叶绿素类二氢卟吩衍生物的合成  

Chemical Reaction of Purpurin-18 Imide and Synthesis of Chlorins Related to Chlorophyll

作　　者：纪建业[1] 夏尚文[2] 赵丽丽[2] 李家柱[2] 祁彩霞 王进军[2,3] 

机构地区：[1]通化师范学院化学系,通化134002 [2]烟台大学化学化工学院,烟台264005 [3]山东省黄金工程技术研究中心(工业应用),烟台264005

出　　处：《有机化学》2013年第7期1457-1464,共8页Chinese Journal of Organic Chemistry

基　　金：国家自然科学基金(No.21272048);山东省黄金工程技术研究中心(2011年度)资助项目~~

摘　　要：以N-甲氧基红紫素-18二酰亚胺甲酯为起始原料,利用其二氢卟吩大环上的活性反应区域,分别进行了3-位乙烯基的亲电加成和1,3-偶极环加成反应、20-meso-位的亲电取代反应、12-位甲基的空气氧化和亲核取代反应的研究,在红紫素-18二酰亚胺周环上的C(3)-,C(12)-和C(20)-meso-位上构建和引进不同的化学结构和取代基团,完成了11个未见报道的叶绿素类二氢卟吩衍生物的合成,其化学结构均经UV,1H NMR,IR及元素分析予以证实;Purpurin-18 imide methyl ester was used as a starting material, and its chemical reactions, including the electro- philic addition and 1,3-polar cycloaddition on the vinyl group at 3-position, the electrophilic substitution at 20-meso-position, the allomerization of C（12）-methyl group and nucleophilic substitution, were carried out making use of the chemical reactivi- ties on the chlorin macrocycle. The different chemical structures and substituent groups were established and introduced at C（3）-, C（12）- and C（20）-meso-potation on the periphery of purpurin-18 imide. The synthesis of 11 unreported chlorins related to chlorophyll was accomplished and their chemical structures were characterized by UV, 1H NMR, IR spectra and elemental analysis. The possible mechanisms about corresponding reactions were tentatively proposed.

关 键 词：叶绿素-A 红紫素-18二酰亚胺 二氢卟吩 化学反应 合成 

分 类 号：O626[理学—有机化学]