2,3,4,6-四-O-苄基井冈霉烯胺的合成  

Synthesis of tetra-O-benzylvalienamine

作　　者：杨光丽[1] 刘侠[1] 张硕[1] 杨劲松[1] 

机构地区：[1]四川大学华西药学院,四川成都610041

出　　处：《化学研究与应用》2009年第5期730-733,共4页Chemical Research and Application

基　　金：国家自然科学基金面上项目(20672074)

摘　　要：Tetra-O-benzylvalienamine was successfully synthesized by taking D-glucose as the starting material via a twelve-steps procedure in an overall yield of 4.7% in this paper.The structure of the title compound was confirmed by spectral analysis.This improved method could avoid the usage of some poisonous reagents,reduce the cost and increase the total yield.Tetra-O-benzylvalienamine was successfully synthesized by taking D-glucose as the starting material via a twelve-steps procedure in an overall yield of 4.7% in this paper. The structure of the title compound was confirmed by spectral analysis. This improved method could avoid the usage of some poisonous reagents, reduce the cost and increase the total yield.

关 键 词：2 3 4 6-四-O-苄基井冈霉烯胺 D-葡萄糖 合成 

分 类 号：O621.3[理学—有机化学]