Efficient and Regioselective 9-Endo Cyclization of alpha-Carbamoyl Radicals

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	Efficient and Regioselective 9-Endo Cyclization of alpha-Carbamoyl Radicals
	Song LY(宋立彦) ; Liu K(刘鲲) ; Li CZ(李超忠)
刊名	Org. Lett.
	2011
卷号	13 期号:13 页码:3434-3437
ISSN号	1523-7060
其他题名	高效及区域选择性的α-酰胺基自由基9-endo环合反应
英文摘要	With the promotion of Lewis acid BF(3)center dot OEt(2), various N-(hex-5-enyl)-2-iodoalkanamides underwent efficient and regioselective 9-endo iodine-atom-transfer radical cyclization reactions at room temperature. The cyclized products were readily converted to the corresponding azonan-2-ones by reduction with Bu(3)SnH or to hexahydroindolizin-3(5H)-ones by treatment with aqueous Na(2)CO(3) in a one-pot, two-stage manner.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/ol201180g
语种	英语
WOS记录号	WOS:000291920800038
公开日期	2013-03-04
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/22864]
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	Song LY,Liu K,Li CZ. Efficient and Regioselective 9-Endo Cyclization of alpha-Carbamoyl Radicals[J]. Org. Lett.,2011,13(13):3434-3437.
APA	宋立彦,刘鲲,&李超忠.(2011).Efficient and Regioselective 9-Endo Cyclization of alpha-Carbamoyl Radicals.Org. Lett.,13(13),3434-3437.
MLA	宋立彦,et al."Efficient and Regioselective 9-Endo Cyclization of alpha-Carbamoyl Radicals".Org. Lett. 13.13(2011):3434-3437.