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.
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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. |
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