Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines
Mao KB(毛可彬) ; Fan GQ(范国钦) ; Liu YH(刘元红) ; Li S(李石) ; You X(尤旭) ; Liu D(刘丹)
刊名Beilstein J. Org. Chem.
2013
卷号9页码:621-627
ISSN号1860-5397
其他题名钛促进的亚胺与端炔的还原偶联反应研究: 烯丙基胺的高效合成
通讯作者刘元红
英文摘要Low-valency titanium species, generated in situ by using Ti(OiPr)(4)/2 c-C5H9MgCl reagent, react with imines to give a titanium-imine complex that can couple with terminal alkynes to provide azatitanacyclopentenes with excellent regioselectivity. Stereode
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.3762/bjoc.9.69
语种英语
WOS记录号WOS:000317282900001
公开日期2014-07-18
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/29187]  
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
Mao KB,Fan GQ,Liu YH,et al. Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines[J]. Beilstein J. Org. Chem.,2013,9:621-627.
APA 毛可彬,范国钦,刘元红,李石,尤旭,&刘丹.(2013).Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines.Beilstein J. Org. Chem.,9,621-627.
MLA 毛可彬,et al."Titanium-mediated reductive cross-coupling reactions of imines with terminal alkynes: An efficient route for the synthesis of stereodefined allylic amines".Beilstein J. Org. Chem. 9(2013):621-627.
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