Zhijun Hao , Jianguo Han , Xiushan Liu , Huifeng Yue
{"title":"铁催化的C-H键通过光诱导配体到金属的电荷转移功能化成肟醚。","authors":"Zhijun Hao , Jianguo Han , Xiushan Liu , Huifeng Yue","doi":"10.1039/d5ob00346f","DOIUrl":null,"url":null,"abstract":"<div><div>We have developed a novel strategy for Fe-catalyzed C–H functionalization into oxime ethers through photo-induced ligand-to-metal charge transfer (LMCT). The method avoids the need for photocatalysts and bases, utilizing a cheap and readily available catalyst under mild conditions. It offers a broad substrate scope, scalability, and high efficiency, providing a promising and cost-effective strategy for synthesizing oxime ethers from simple and abundant starting materials.</div></div>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":"23 43","pages":"Pages 9823-9827"},"PeriodicalIF":2.8000,"publicationDate":"2025-06-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Iron-catalyzed C–H bond functionalization into oxime ethers via photo-induced ligand-to-metal charge transfer†\",\"authors\":\"Zhijun Hao , Jianguo Han , Xiushan Liu , Huifeng Yue\",\"doi\":\"10.1039/d5ob00346f\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>We have developed a novel strategy for Fe-catalyzed C–H functionalization into oxime ethers through photo-induced ligand-to-metal charge transfer (LMCT). The method avoids the need for photocatalysts and bases, utilizing a cheap and readily available catalyst under mild conditions. It offers a broad substrate scope, scalability, and high efficiency, providing a promising and cost-effective strategy for synthesizing oxime ethers from simple and abundant starting materials.</div></div>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\"23 43\",\"pages\":\"Pages 9823-9827\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-06-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1477052025008201\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/4/2 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1477052025008201","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/4/2 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Iron-catalyzed C–H bond functionalization into oxime ethers via photo-induced ligand-to-metal charge transfer†
We have developed a novel strategy for Fe-catalyzed C–H functionalization into oxime ethers through photo-induced ligand-to-metal charge transfer (LMCT). The method avoids the need for photocatalysts and bases, utilizing a cheap and readily available catalyst under mild conditions. It offers a broad substrate scope, scalability, and high efficiency, providing a promising and cost-effective strategy for synthesizing oxime ethers from simple and abundant starting materials.
期刊介绍:
Organic & Biomolecular Chemistry is an international journal using integrated research in chemistry-organic chemistry. Founded in 2003 by the Royal Society of Chemistry, the journal is published in Semimonthly issues and has been indexed by SCIE, a leading international database. The journal focuses on the key research and cutting-edge progress in the field of chemistry-organic chemistry, publishes and reports the research results in this field in a timely manner, and is committed to becoming a window and platform for rapid academic exchanges among peers in this field. The journal's impact factor in 2023 is 2.9, and its CiteScore is 5.5.