Biomimetic Cationic Cyclization toward ent-Kaurene-type Diterpenoids

	Biomimetic Cationic Cyclization toward ent-Kaurene-type Diterpenoids
	Zhu LL(朱莉莉) ; Hong R(洪然)
刊名	Chin. J. Chem.
	2013
卷号	31 期号:1 页码:111-118
ISSN号	1001-604X
其他题名	对映-贝壳杉烯二萜类化合物的仿生碳阳离子环化研究
通讯作者	洪然
英文摘要	Terpenoids comprise the largest family of natural products and include various structurally different genus which play important roles in living organisms. Biosynthetically, diterpenoids are derived from (E,E,E)-geranylgeranyl diphosphate (GGPP). From GGP
学科主题	天然产物有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/cjoc.201201029
语种	英语
WOS记录号	WOS:000313811800022
公开日期	2014-10-15
内容类型	期刊论文
源URL	[http://ir.sioc.ac.cn/handle/331003/29265]
专题	上海有机化学研究所_中科院天然产物有机化学重点实验室
推荐引用方式 GB/T 7714	Zhu LL,Hong R. Biomimetic Cationic Cyclization toward ent-Kaurene-type Diterpenoids[J]. Chin. J. Chem.,2013,31(1):111-118.
APA	朱莉莉,&洪然.(2013).Biomimetic Cationic Cyclization toward ent-Kaurene-type Diterpenoids.Chin. J. Chem.,31(1),111-118.
MLA	朱莉莉,et al."Biomimetic Cationic Cyclization toward ent-Kaurene-type Diterpenoids".Chin. J. Chem. 31.1(2013):111-118.