Ring-opening of N-tosylaziridines with TMSN^3 and TMSCN Triggered by TBAF: An efficient and convenient route to vicinal diamines and β=aminoacid

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	Ring-opening of N-tosylaziridines with TMSN^3 and TMSCN Triggered by TBAF: An efficient and convenient route to vicinal diamines and β=aminoacid
	Wu J(吴诘) ; Hou XL(侯雪龙) ; Dai LX(戴立信)
刊名	J. Org. Chem.
	2000
卷号	65 期号:5 页码:1344-1348
ISSN号	0022-3263
其他题名	TBAF 引发的 TMSN^3和TMSCN对N-对甲苯磺酰基氮杂环丙烷的开环反应: 一个有效的制备邻二胺及β-氨基酸的方法
通讯作者	侯雪龙
英文摘要	Ring-opening reactions of aziridines with trimethylsilyl compounds triggered by tetrabutylammonium fluoride give the corresponding products regioselectively in excellent yield. It provides a facile and efficient procedure for the ring-opening reactions of aziridines and affords a practical access to the synthesis of cyano-, azido-, or chloroamines because of its efficiency and simplicity. The products are easily transformed to vicinal diamines or β-amino acids.
学科主题	有机化学
收录类别	SCI
原文出处	http://dx.doi.org/10.1021/jo9913816
语种	英语
公开日期	2013-02-19
内容类型	期刊论文
源URL	[http://202.127.28.38/handle/331003/15833]
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	Wu J,Hou XL,Dai LX. Ring-opening of N-tosylaziridines with TMSN^3 and TMSCN Triggered by TBAF: An efficient and convenient route to vicinal diamines and β=aminoacid[J]. J. Org. Chem.,2000,65(5):1344-1348.
APA	吴诘,侯雪龙,&戴立信.(2000).Ring-opening of N-tosylaziridines with TMSN^3 and TMSCN Triggered by TBAF: An efficient and convenient route to vicinal diamines and β=aminoacid.J. Org. Chem.,65(5),1344-1348.
MLA	吴诘,et al."Ring-opening of N-tosylaziridines with TMSN^3 and TMSCN Triggered by TBAF: An efficient and convenient route to vicinal diamines and β=aminoacid".J. Org. Chem. 65.5(2000):1344-1348.