通过 C-S 和 C-H 键活化,钯催化α-芳基噻蒽盐与亚磺酰基锍的芳基化反应。

IF 3.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Prof. Qing-Dong Wang, Xue Chen, Yuan-Shuai Wu, Prof. Chengping Miao, Prof. Jin-Ming Yang, Prof. Zhi-Liang Shen
{"title":"通过 C-S 和 C-H 键活化,钯催化α-芳基噻蒽盐与亚磺酰基锍的芳基化反应。","authors":"Prof. Qing-Dong Wang,&nbsp;Xue Chen,&nbsp;Yuan-Shuai Wu,&nbsp;Prof. Chengping Miao,&nbsp;Prof. Jin-Ming Yang,&nbsp;Prof. Zhi-Liang Shen","doi":"10.1002/asia.202401873","DOIUrl":null,"url":null,"abstract":"<p>Diverse <i>α</i>-aryl <i>α</i>-carbonyl sulfoxonium ylides were efficiently synthesized in yields ranging from moderate to high via a palladium-catalyzed <i>α</i>-arylation of sulfoxonium ylides with aryl thianthrenium salts. The reactions proceeded smoothly via C−S and C−H bond functionalization, exhibiting broad substrate scope and good compatibility to various functionalities. In addition, the scale-up synthesis could be achieved, and the one-pot protocol commencing from the use of simple arene as the precursor of aryl thianthrenium salt could also be accomplished.</p>","PeriodicalId":145,"journal":{"name":"Chemistry - An Asian Journal","volume":"20 10","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Palladium–Catalyzed α-Arylation of Sulfoxonium Ylides with Aryl Thianthrenium Salts via C−S and C−H Bond Activation\",\"authors\":\"Prof. Qing-Dong Wang,&nbsp;Xue Chen,&nbsp;Yuan-Shuai Wu,&nbsp;Prof. Chengping Miao,&nbsp;Prof. Jin-Ming Yang,&nbsp;Prof. Zhi-Liang Shen\",\"doi\":\"10.1002/asia.202401873\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Diverse <i>α</i>-aryl <i>α</i>-carbonyl sulfoxonium ylides were efficiently synthesized in yields ranging from moderate to high via a palladium-catalyzed <i>α</i>-arylation of sulfoxonium ylides with aryl thianthrenium salts. The reactions proceeded smoothly via C−S and C−H bond functionalization, exhibiting broad substrate scope and good compatibility to various functionalities. In addition, the scale-up synthesis could be achieved, and the one-pot protocol commencing from the use of simple arene as the precursor of aryl thianthrenium salt could also be accomplished.</p>\",\"PeriodicalId\":145,\"journal\":{\"name\":\"Chemistry - An Asian Journal\",\"volume\":\"20 10\",\"pages\":\"\"},\"PeriodicalIF\":3.3000,\"publicationDate\":\"2025-02-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry - An Asian Journal\",\"FirstCategoryId\":\"1\",\"ListUrlMain\":\"https://aces.onlinelibrary.wiley.com/doi/10.1002/asia.202401873\",\"RegionNum\":3,\"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":"Chemistry - An Asian Journal","FirstCategoryId":"1","ListUrlMain":"https://aces.onlinelibrary.wiley.com/doi/10.1002/asia.202401873","RegionNum":3,"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

通过钯催化亚砜鎓化物与芳基硫鎓盐的α-芳基芳化反应,以中高收率合成了多种α-芳基α-羰基亚砜鎓化物。通过C-S键和C-H键功能化反应进行顺利,具有广泛的底物范围和对各种官能团的良好相容性。此外,还可实现规模化合成,并可实现以简单芳烃为前驱体的一锅法合成芳基硫鎓盐。
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 α-Arylation of Sulfoxonium Ylides with Aryl Thianthrenium Salts via C−S and C−H Bond Activation

Palladium–Catalyzed α-Arylation of Sulfoxonium Ylides with Aryl Thianthrenium Salts via C−S and C−H Bond Activation

Palladium–Catalyzed α-Arylation of Sulfoxonium Ylides with Aryl Thianthrenium Salts via C−S and C−H Bond Activation

Palladium–Catalyzed α-Arylation of Sulfoxonium Ylides with Aryl Thianthrenium Salts via C−S and C−H Bond Activation

Diverse α-aryl α-carbonyl sulfoxonium ylides were efficiently synthesized in yields ranging from moderate to high via a palladium-catalyzed α-arylation of sulfoxonium ylides with aryl thianthrenium salts. The reactions proceeded smoothly via C−S and C−H bond functionalization, exhibiting broad substrate scope and good compatibility to various functionalities. In addition, the scale-up synthesis could be achieved, and the one-pot protocol commencing from the use of simple arene as the precursor of aryl thianthrenium salt could also be accomplished.

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
Chemistry - An Asian Journal
Chemistry - An Asian Journal 化学-化学综合
CiteScore
7.00
自引率
2.40%
发文量
535
审稿时长
1.3 months
期刊介绍: Chemistry—An Asian Journal is an international high-impact journal for chemistry in its broadest sense. The journal covers all aspects of chemistry from biochemistry through organic and inorganic chemistry to physical chemistry, including interdisciplinary topics. Chemistry—An Asian Journal publishes Full Papers, Communications, and Focus Reviews. A professional editorial team headed by Dr. Theresa Kueckmann and an Editorial Board (headed by Professor Susumu Kitagawa) ensure the highest quality of the peer-review process, the contents and the production of the journal. Chemistry—An Asian Journal is published on behalf of the Asian Chemical Editorial Society (ACES), an association of numerous Asian chemical societies, and supported by the Gesellschaft Deutscher Chemiker (GDCh, German Chemical Society), ChemPubSoc Europe, and the Federation of Asian Chemical Societies (FACS).
×
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