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学科主题: 药学
题名:
Direct Access to Tetrahydro[1,2]diazepinones from alpha,beta-Epoxy-N-aziridinylimines via Anionic Rearrangement
作者: Wu, Fufang1,3,4; Dong, Min2; Fang, Fang4; Sang, Yingxia4; Li, Yun3; Cheng, Bin3,4; Zhang, Lihe2; Zhai, Hongbin3
刊名: ORGANIC LETTERS
发表日期: 2013-02-15
DOI: 10.1021/ol400070j
卷: 15, 期:4, 页:914-916
收录类别: SCI ; IC ; CCR
文章类型: Article
WOS标题词: Science & Technology
类目[WOS]: Chemistry, Organic
研究领域[WOS]: Chemistry
关键词[WOS]: N-AZIRIDINYL IMINES ; BOND FORMATION APPROACH ; RADICAL CYCLIZATION ; EFFICIENT SYNTHESIS ; ROUTE ; LITHIATION ; REAGENTS ; CARBONYL ; KETONES
英文摘要:

A novel one-step synthetic approach to tetrahydro[1,2]diazepinones via base-promoted rearrangement of alpha,beta-epoxy-N-aziridinylimines, derived from alpha,beta-epoxyketones and N-aminoaziridines, has been developed.

语种: 英语
所属项目编号: 2010CB833200 ; 21172100 ; 21272105 ; 21290183 ; IRT1138
项目资助者: National Basic Research Program of China (973 Program) ; NSFC ; Program for Changjiang Scholars and Innovative Research Team in University (PCSIRT) ; MOE
WOS记录号: WOS:000315254500050
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.bjmu.edu.cn/handle/400002259/57562
Appears in Collections:北京大学药学院_期刊论文

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作者单位: 1.Univ Sci & Technol China, Dept Chem, Hefei 230026, Peoples R China
2.Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
3.Lanzhou Univ, State Key Lab Appl Organ Chem, Lanzhou 730000, Peoples R China
4.Chinese Acad Sci, Shanghai Inst Organ Chem, CAS Key Lab Synthet Chem Nat Subst, Shanghai 200032, Peoples R China

Recommended Citation:
Wu, Fufang,Dong, Min,Fang, Fang,et al. Direct Access to Tetrahydro[1,2]diazepinones from alpha,beta-Epoxy-N-aziridinylimines via Anionic Rearrangement[J]. ORGANIC LETTERS,2013,15(4):914-916.
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