摘要
以芒果苷、氯苄或对氯氯苄为原料,设计并合成了2个3,6,7-O-三取代芒果苷衍生物,收率分别为55%、57%,结构均经核磁共振氢谱确证。制备方法简便,收率较高。
Using mangiferin, 1-chloromethylbenzene or p-chlorobenzylchloride as starting materials, two kinds of 3,6,7-O-trisubstituted derivatives of mangiferin were synthesized with yield of 55%, 57 %, respectively,and their structures were all confirmed by 1HNMR. The preparation method was simple with a high yield.
出处
《化学与生物工程》
CAS
2010年第5期49-50,共2页
Chemistry & Bioengineering
关键词
芒果苷
衍生物
制备
mangiferin
derivative
preparation
