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A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes
Alternative TitleA new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes
Yan ZH(严兆华)1; Xu Y(许云)1; Tian WS(田伟生)1
2014
Source PublicationTetrahedron Lett.
Volume55Issue:52Pages:7186-7189
AbstractThe 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.
Subject Area天然产物有机化学
DOI10.1016/j.tetlet.2014.10.154
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Indexed BySCI
Language英语
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Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38994
Collection中科院天然产物有机化学重点实验室
Corresponding AuthorTian WS(田伟生)
Affiliation1.南昌大学
2.中科院上海有机化学研究所
Recommended Citation
GB/T 7714
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.
APA 严兆华,许云,&田伟生.(2014).A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes.Tetrahedron Lett.,55(52),7186-7189.
MLA 严兆华,et al."A new and concise way to enamides by fluoroalkanosulfonyl fluoride mediated Beckmann rearrangement of alpha,beta-unsaturated ketoximes".Tetrahedron Lett. 55.52(2014):7186-7189.
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