Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives

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

	Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives
	Ma SM(麻生明) ; Ni BK(倪步阔)
刊名	Chem.-Eur. J.
	2004
卷号	10 期号:13 页码:3286-3300
ISSN号	0947-6539
其他题名	含N烯化合物的双RCM反应。双环化合物的合成及其lupinine 四个立体异构体及其衍生物的合成
通讯作者	麻生明
英文摘要	The double ring-closing metathesis reaction of nitrogen-containing tetraenes was studied. The selectivity of the fused/dumbbell-type products can be controlled by the electronic/steric effects of the substituents attached to the C = C bonds and the s-cis/s-trans conformational ratios of the substrates. This methodology has also been successfully applied to the enantioselective synthesis of four stereoisomers of lupinine and their derivatives.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1002/chem.200305581
语种	英语
WOS记录号	WOS:000222651700019
公开日期	2013-01-15
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/11968]
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. Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives[J]. Chem.-Eur. J.,2004,10(13):3286-3300.
APA	麻生明,&倪步阔.(2004).Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives.Chem.-Eur. J.,10(13),3286-3300.
MLA	麻生明,et al."Double ring-closing metathesis reaction of nitrogen-containing tetraenes: Efficient construction of bicyclic alkaloid skeletons and synthetic application to four stereoisomers of lupinine and their derivatives".Chem.-Eur. J. 10.13(2004):3286-3300.