Synthesis of bisabolane sesquiterpenes: A Johnson-Claisen rearrangement approach

被引:7
|
作者
Du, Zhen Ting [1 ]
Yu, Hong Rui [1 ]
Xu, Yan [1 ]
Li, Yong [1 ]
Li, An Pai [2 ]
机构
[1] NW A&F Univ, Coll Sci, Yangling 712100, Peoples R China
[2] Synthet Technol Pte Ltd, Singapore 048693, Singapore
基金
中国国家自然科学基金;
关键词
Bisabolane sesquiterpenes; Johnson-Claisen rearrangement; Synthesis; ENANTIOSELECTIVE SYNTHESIS; ETHER; (+/-)-CURCUPHENOL; (+)-CURCUPHENOL; TERPENOIDS;
D O I
10.1016/j.cclet.2010.02.024
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Several bisabolane sesquiterpenes, (+/-)-curcumene, (+/-)-curcuphenol, (+/-)-curcudiol and (+/-)-curcuhydroquinone, have been synthesized in racemic form and fully characterized. The salient characteristic of our approach is that a Johnson-Claisen arrangement was involved as a key step. (C) 2010 Zhen Ting Du. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
引用
收藏
页码:813 / 815
页数:3
相关论文
共 50 条