Tf2O/DMSO-Promoted Umpolung Phosphorylation for C(sp2)–P or C(sp3)–P Bond Formation

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC Journal of Organic Chemistry Pub Date : 2025-04-10 DOI:10.1021/acs.joc.5c00262
Da-Wei Shi, Ming Li, Rui-Jia Yang, Xin-Yu Zhao, Ting Zhang, Jiayi Huangfu, Ling Xu, Ke Wang, Yi-Xuan Ma, Bin Yang
{"title":"Tf2O/DMSO-Promoted Umpolung Phosphorylation for C(sp2)–P or C(sp3)–P Bond Formation","authors":"Da-Wei Shi, Ming Li, Rui-Jia Yang, Xin-Yu Zhao, Ting Zhang, Jiayi Huangfu, Ling Xu, Ke Wang, Yi-Xuan Ma, Bin Yang","doi":"10.1021/acs.joc.5c00262","DOIUrl":null,"url":null,"abstract":"We have developed an umpolung method utilizing the Tf<sub>2</sub>O/DMSO-based system for C(sp<sup>2</sup>)–P bond or C(sp<sup>3</sup>)–P bond formation. This method employs both P(O)–H and P(O)–OH compounds as phosphorus sources and demonstrates excellent compatibility with a wide range of Grignard reagents. Without the requirement of precious transition metals or additives, this one-pot protocol provides a practical and efficient synthetic pathway to a variety of aryl and alkyl phosphine oxides. The broad substrate scope and diverse synthetic applications highlight the practical utility of this method.","PeriodicalId":57,"journal":{"name":"Journal of Organic Chemistry","volume":"195 1","pages":""},"PeriodicalIF":3.6000,"publicationDate":"2025-04-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Organic Chemistry","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.joc.5c00262","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0

Abstract

We have developed an umpolung method utilizing the Tf2O/DMSO-based system for C(sp2)–P bond or C(sp3)–P bond formation. This method employs both P(O)–H and P(O)–OH compounds as phosphorus sources and demonstrates excellent compatibility with a wide range of Grignard reagents. Without the requirement of precious transition metals or additives, this one-pot protocol provides a practical and efficient synthetic pathway to a variety of aryl and alkyl phosphine oxides. The broad substrate scope and diverse synthetic applications highlight the practical utility of this method.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Tf2O/DMSO 促进乌普隆磷酸化以形成 C(sp2)-P 或 C(sp3)-P 键
我们开发了一种基于Tf2O/ dmso系统的C(sp2) -P键或C(sp3) -P键形成的umpolung方法。该方法采用P(O) -H和P(O) -OH化合物作为磷源,并与多种格氏试剂具有良好的相容性。在不需要贵重过渡金属或添加剂的情况下,这种一锅法为多种芳基和烷基膦氧化物的合成提供了一条实用高效的途径。广泛的衬底范围和不同的合成应用突出了该方法的实用性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
期刊介绍: Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.
期刊最新文献
Synthesis of Polysubstituted Pyrroles via (2 + 2 + 1) Cyclization of Enone Oxime Ethers with Alkynes and Diaziridinone A Biomimetic Study of the Behavior of N-Cyclopropyl-Based Single Electron Transfer Probes in the Context of Monoamine Oxidase-Catalyzed Oxidations Issue Publication Information Issue Editorial Masthead Context Rules! Special Issue on “Physical Organic Chemistry: Never Out of Style”
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1