光诱导铁催化C(sp2)-O交叉偶联羧酸与茴香醚合成芳基酯

IF 13.1 1区 化学 Q1 CHEMISTRY, PHYSICAL
Jaya Tripathi, Anuj Sharma
{"title":"光诱导铁催化C(sp2)-O交叉偶联羧酸与茴香醚合成芳基酯","authors":"Jaya Tripathi, Anuj Sharma","doi":"10.1021/acscatal.5c04512","DOIUrl":null,"url":null,"abstract":"An efficient method for the synthesis of aryl esters was developed using photoinduced iron catalysis. The carboxylation of abundantly available anisoles proceeds via an aromatic radical substitution pathway. A broad range of carboxylic acids and anisoles were successfully coupled to afford aryl esters in moderate to good yields. Mechanistic studies revealed that (i) Fe(III) is reduced to Fe(II) along with the generation of a chloride radical through a visible-light-induced ligand-to-metal charge transfer (LMCT) process; (ii) the carboxy radical is formed via hydrogen atom transfer (HAT) from the carboxylic acid to the chloride radical; (iii) Fe(III) promotes <i>ipso</i>-substitution by interacting with the electronegative oxygen atom of the anisole to facilitate the aryl esters synthesis.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":"109 1","pages":""},"PeriodicalIF":13.1000,"publicationDate":"2025-10-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoinduced Iron-Catalyzed Aryl Ester Synthesis via C(sp2)-O Cross-Coupling of Carboxylic Acids with Anisoles\",\"authors\":\"Jaya Tripathi, Anuj Sharma\",\"doi\":\"10.1021/acscatal.5c04512\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An efficient method for the synthesis of aryl esters was developed using photoinduced iron catalysis. The carboxylation of abundantly available anisoles proceeds via an aromatic radical substitution pathway. A broad range of carboxylic acids and anisoles were successfully coupled to afford aryl esters in moderate to good yields. Mechanistic studies revealed that (i) Fe(III) is reduced to Fe(II) along with the generation of a chloride radical through a visible-light-induced ligand-to-metal charge transfer (LMCT) process; (ii) the carboxy radical is formed via hydrogen atom transfer (HAT) from the carboxylic acid to the chloride radical; (iii) Fe(III) promotes <i>ipso</i>-substitution by interacting with the electronegative oxygen atom of the anisole to facilitate the aryl esters synthesis.\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":\"109 1\",\"pages\":\"\"},\"PeriodicalIF\":13.1000,\"publicationDate\":\"2025-10-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acscatal.5c04512\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acscatal.5c04512","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

摘要

研究了光诱导铁催化合成芳基酯的有效方法。大量可用茴香醚的羧基化是通过芳基取代途径进行的。广泛的羧酸和茴香醚成功地偶联,以中等到良好的产量提供芳基酯。机理研究表明:(1)Fe(III)通过可见光诱导的配体-金属电荷转移(LMCT)过程被还原为Fe(II),同时生成氯自由基;(ii)羧基通过从羧酸到氯基的氢原子转移(HAT)形成;(iii) Fe(iii)通过与苯甲醚的电负性氧原子相互作用促进对映基取代,促进芳基酯的合成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Photoinduced Iron-Catalyzed Aryl Ester Synthesis via C(sp2)-O Cross-Coupling of Carboxylic Acids with Anisoles

Photoinduced Iron-Catalyzed Aryl Ester Synthesis via C(sp2)-O Cross-Coupling of Carboxylic Acids with Anisoles
An efficient method for the synthesis of aryl esters was developed using photoinduced iron catalysis. The carboxylation of abundantly available anisoles proceeds via an aromatic radical substitution pathway. A broad range of carboxylic acids and anisoles were successfully coupled to afford aryl esters in moderate to good yields. Mechanistic studies revealed that (i) Fe(III) is reduced to Fe(II) along with the generation of a chloride radical through a visible-light-induced ligand-to-metal charge transfer (LMCT) process; (ii) the carboxy radical is formed via hydrogen atom transfer (HAT) from the carboxylic acid to the chloride radical; (iii) Fe(III) promotes ipso-substitution by interacting with the electronegative oxygen atom of the anisole to facilitate the aryl esters synthesis.
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
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
×
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