Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis

IF 51.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Lauren E. Ehehalt, Omar M. Beleh, Isabella C. Priest, Julianna M. Mouat, Alyssa K. Olszewski, Benjamin N. Ahern, Alexandro R. Cruz, Benjamin K. Chi, Anthony J. Castro, Kai Kang, Jiang Wang and Daniel J. Weix*, 
{"title":"Cross-Electrophile Coupling: Principles, Methods, and Applications in Synthesis","authors":"Lauren E. Ehehalt,&nbsp;Omar M. Beleh,&nbsp;Isabella C. Priest,&nbsp;Julianna M. Mouat,&nbsp;Alyssa K. Olszewski,&nbsp;Benjamin N. Ahern,&nbsp;Alexandro R. Cruz,&nbsp;Benjamin K. Chi,&nbsp;Anthony J. Castro,&nbsp;Kai Kang,&nbsp;Jiang Wang and Daniel J. Weix*,&nbsp;","doi":"10.1021/acs.chemrev.4c0052410.1021/acs.chemrev.4c00524","DOIUrl":null,"url":null,"abstract":"<p >Cross-electrophile coupling (XEC), defined by us as the cross-coupling of two different σ-electrophiles that is driven by catalyst reduction, has seen rapid progression in recent years. As such, this review aims to summarize the field from its beginnings up until mid-2023 and to provide comprehensive coverage on synthetic methods and current state of mechanistic understanding. Chapters are split by type of bond formed, which include C(sp<sup>3</sup>)–C(sp<sup>3</sup>), C(sp<sup>2</sup>)–C(sp<sup>2</sup>), C(sp<sup>2</sup>)–C(sp<sup>3</sup>), and C(sp<sup>2</sup>)–C(sp) bond formation. Additional chapters include alkene difunctionalization, alkyne difunctionalization, and formation of carbon-heteroatom bonds. Each chapter is generally organized with an initial summary of mechanisms followed by detailed figures and notes on methodological developments and ending with application notes in synthesis. While XEC is becoming an increasingly utilized approach in synthesis, its early stage of development means that optimal catalysts, ligands, additives, and reductants are still in flux. This review has collected data on these and various other aspects of the reactions to capture the state of the field. Finally, the data collected on the papers in this review is offered as Supporting Information for readers.</p>","PeriodicalId":32,"journal":{"name":"Chemical Reviews","volume":"124 23","pages":"13397–13569 13397–13569"},"PeriodicalIF":51.4000,"publicationDate":"2024-11-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.acs.org/doi/epdf/10.1021/acs.chemrev.4c00524","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical Reviews","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.chemrev.4c00524","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

Abstract

Cross-electrophile coupling (XEC), defined by us as the cross-coupling of two different σ-electrophiles that is driven by catalyst reduction, has seen rapid progression in recent years. As such, this review aims to summarize the field from its beginnings up until mid-2023 and to provide comprehensive coverage on synthetic methods and current state of mechanistic understanding. Chapters are split by type of bond formed, which include C(sp3)–C(sp3), C(sp2)–C(sp2), C(sp2)–C(sp3), and C(sp2)–C(sp) bond formation. Additional chapters include alkene difunctionalization, alkyne difunctionalization, and formation of carbon-heteroatom bonds. Each chapter is generally organized with an initial summary of mechanisms followed by detailed figures and notes on methodological developments and ending with application notes in synthesis. While XEC is becoming an increasingly utilized approach in synthesis, its early stage of development means that optimal catalysts, ligands, additives, and reductants are still in flux. This review has collected data on these and various other aspects of the reactions to capture the state of the field. Finally, the data collected on the papers in this review is offered as Supporting Information for readers.

求助全文
约1分钟内获得全文 求助全文
来源期刊
Chemical Reviews
Chemical Reviews 化学-化学综合
CiteScore
106.00
自引率
1.10%
发文量
278
审稿时长
4.3 months
期刊介绍: Chemical Reviews is a highly regarded and highest-ranked journal covering the general topic of chemistry. Its mission is to provide comprehensive, authoritative, critical, and readable reviews of important recent research in organic, inorganic, physical, analytical, theoretical, and biological chemistry. Since 1985, Chemical Reviews has also published periodic thematic issues that focus on a single theme or direction of emerging 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:481959085
Book学术官方微信