钯催化脲系烯烃的氨基炔化/烯烯化反应:获得含炔和烯的咪唑烷酮

IF 4.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Qianqian Hu, Cangzhu Hu, Tian Tang, Qing Wu, Weiming Hu, Qiang Dai, Lei Wang
{"title":"钯催化脲系烯烃的氨基炔化/烯烯化反应:获得含炔和烯的咪唑烷酮","authors":"Qianqian Hu, Cangzhu Hu, Tian Tang, Qing Wu, Weiming Hu, Qiang Dai, Lei Wang","doi":"10.1039/d5cc04327a","DOIUrl":null,"url":null,"abstract":"A novel palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes has been developed, offering an efficient strategy for the synthesis of imidazolidinones bearing alkyne and allene in moderate to good yields. The reaction exhibits broad substrate scope, excellent functional group tolerance and well synthetic versatility.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"68 1","pages":""},"PeriodicalIF":4.2000,"publicationDate":"2025-10-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium catalyzed aminoalkynylation/alleneamination of ureatethered alkenes:access to imidazolidinones bearing alkyne and allene\",\"authors\":\"Qianqian Hu, Cangzhu Hu, Tian Tang, Qing Wu, Weiming Hu, Qiang Dai, Lei Wang\",\"doi\":\"10.1039/d5cc04327a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A novel palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes has been developed, offering an efficient strategy for the synthesis of imidazolidinones bearing alkyne and allene in moderate to good yields. The reaction exhibits broad substrate scope, excellent functional group tolerance and well synthetic versatility.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"68 1\",\"pages\":\"\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-10-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5cc04327a\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5cc04327a","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

研究了一种新的钯催化脲系烯烃氨基炔化/烯丙烯化反应,为中高收率合成含炔和烯丙烯的咪唑烷酮提供了一条有效途径。该反应具有广泛的底物范围、良好的官能团耐受性和良好的合成通用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Palladium catalyzed aminoalkynylation/alleneamination of ureatethered alkenes:access to imidazolidinones bearing alkyne and allene
A novel palladium-catalyzed aminoalkynylation/alleneamination of urea-tethered alkenes has been developed, offering an efficient strategy for the synthesis of imidazolidinones bearing alkyne and allene in moderate to good yields. The reaction exhibits broad substrate scope, excellent functional group tolerance and well synthetic versatility.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信