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学科主题: 天然产物有机化学
题名: A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes
其他题名: A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes
作者: Yan ZH(严兆华)1; Xu Y(许云)1; Tian WS(田伟生)1
通讯作者: 田伟生
刊名: Tetrahedron Lett.
发表日期: 2014
DOI: 10.1016/j.tetlet.2014.10.154
卷: 55, 期:52, 页:7186-7189
收录类别: SCI
英文摘要: The reaction of alpha,beta-unsaturated ketoximes with fluoroalkanosulfonyl fluorides in the presence of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) underwent the Beckmann rearrangement smoothly to afford the corresponding acid-sensitive enamides in moderate to excellent yields, which provides a new efficient method for the preparation of acid-sensitive enamides. (C) 2014 Elsevier Ltd. All rights reserved.
语种: 英语
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内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/38994
Appears in Collections:中科院天然产物有机化学重点实验室_期刊论文

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作者单位: 1.南昌大学
2.中科院上海有机化学研究所

Recommended Citation:
Yan ZH,Xu Y,Tian WS. A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes[J]. Tetrahedron Lett.,2014,55(52):7186-7189.
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