Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core

CORC > 上海有机化学研究所 > 中国科学院上海有机化学研究所 > 金属有机化学国家重点实验室

	Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core
	Ma SM(麻生明) ; Ni BK(倪步阔)
刊名	J. Org. Chem.
	2002
卷号	67 期号:23 页码:8280-8283
ISSN号	0022-3263
其他题名	分子内三Heck反应. 一种以苯为母核的四环化合物的合成
通讯作者	麻生明
英文摘要	Twelve examples of 1,3,5-tribromo-2,4,6-trienylbenzenes were easily synthesized by alkylation, etherification, and amination methods. Under conditions A and B, a series of tetracycles with a benzene core, I.e., fused 5,6,6-6.6.6-, and 6,6,7-tetracyclic compounds, were prepared efficiently via this intramolecular triple Heck reaction protocol.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/jo0258094
语种	英语
WOS记录号	WOS:000179110400053
公开日期	2013-01-15
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/11898]
专题	上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式 GB/T 7714	Ma SM,Ni BK. Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core[J]. J. Org. Chem.,2002,67(23):8280-8283.
APA	麻生明,&倪步阔.(2002).Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core.J. Org. Chem.,67(23),8280-8283.
MLA	麻生明,et al."Intramolecular triple heck reaction. An efficient entry to fused tetracycles with a benzene core".J. Org. Chem. 67.23(2002):8280-8283.