SIOC OpenIR  > 高分子材料研究室
Synthesis of alpha-Methylene-beta-Lactams via PPh3-Catalyzed Umpolung Cyclization of Propiolamides
Alternative Title由三苯膦催化的丙酰胺极性反转环合合成alpha-亚甲基-beta-内酰胺
Zhu L(朱林)1; Xiong Y(熊彦)1; Li CZ(李超忠)1
2015
Source PublicationJ. Org. Chem.
Volume80Issue:1Pages:628-633
AbstractWe report herein a facile synthesis of alpha-methylene-beta lactams. Thus, under the catalysis of triphenylphosphine, a number of 2-propiolamidoacetates or alpha-propiolamido ketones in refluxing ethanol underwent umpolung cyclization to afford the corresponding 4-substituted 3-methyleneazetidin-2-ones in high yields.
Subtype论文
Subject Area高分子化学
DOI10.1021/jo502265a
URL查看原文
Indexed BySCI
Language英语
WOS IDWOS:000347506400064
Citation statistics
Cited Times:17[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/39829
Collection高分子材料研究室
Corresponding AuthorLi CZ(李超忠)
Affiliation1.中国科学技术大学
2.中科院上海有机化学研究所
Recommended Citation
GB/T 7714
Zhu L,Xiong Y,Li CZ. Synthesis of alpha-Methylene-beta-Lactams via PPh3-Catalyzed Umpolung Cyclization of Propiolamides[J]. J. Org. Chem.,2015,80(1):628-633.
APA 朱林,熊彦,&李超忠.(2015).Synthesis of alpha-Methylene-beta-Lactams via PPh3-Catalyzed Umpolung Cyclization of Propiolamides.J. Org. Chem.,80(1),628-633.
MLA 朱林,et al."Synthesis of alpha-Methylene-beta-Lactams via PPh3-Catalyzed Umpolung Cyclization of Propiolamides".J. Org. Chem. 80.1(2015):628-633.
Files in This Item:
File Name/Size DocType Version Access License
2015005.pdf(327KB)期刊论文作者接受稿开放获取CC BY-NC-SAApplication Full Text
Related Services
Recommend this item
Bookmark
Usage statistics
Export to Endnote
Google Scholar
Similar articles in Google Scholar
[朱林]'s Articles
[熊彦]'s Articles
[李超忠]'s Articles
Baidu academic
Similar articles in Baidu academic
[朱林]'s Articles
[熊彦]'s Articles
[李超忠]'s Articles
Bing Scholar
Similar articles in Bing Scholar
[朱林]'s Articles
[熊彦]'s Articles
[李超忠]'s Articles
Terms of Use
No data!
Social Bookmark/Share
All comments (0)
No comment.
 

Items in the repository are protected by copyright, with all rights reserved, unless otherwise indicated.