Stereoselective 6-Exo Cyclization of Amidyl Radicals. An Experimental and Theoretical Study

	Stereoselective 6-Exo Cyclization of Amidyl Radicals. An Experimental and Theoretical Study
	Zhuang SJ(庄顺君) ; Liu K(刘鲲) ; Li CZ(李超忠)
刊名	J. Org. Chem.
	2011
卷号	76 期号:19 页码:8100-8106
ISSN号	0022-3263
其他题名	立体选择性的酰胺氮自由基6-exo环合反应的实验和理论研究
通讯作者	刘鲲 ; 李超忠
英文摘要	Unsaturated primary arnidyl radicals of Z-configurations underwent efficient chemo-and stereoselective 6-exo cyclization reactions via chair-conformational transition states, leading to the predominant formations of 3,6-trans, 4,6-cis, or 5,6-trans substituted delta-lactams.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/jo2014406
语种	英语
WOS记录号	WOS:000295302300054
公开日期	2013-03-04
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/22866]
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	Zhuang SJ,Liu K,Li CZ. Stereoselective 6-Exo Cyclization of Amidyl Radicals. An Experimental and Theoretical Study[J]. J. Org. Chem.,2011,76(19):8100-8106.
APA	庄顺君,刘鲲,&李超忠.(2011).Stereoselective 6-Exo Cyclization of Amidyl Radicals. An Experimental and Theoretical Study.J. Org. Chem.,76(19),8100-8106.
MLA	庄顺君,et al."Stereoselective 6-Exo Cyclization of Amidyl Radicals. An Experimental and Theoretical Study".J. Org. Chem. 76.19(2011):8100-8106.