{"title":"n -乙烯酰亚胺与烷基、硅基和酰基自由基的模块化还原自由基-极性交叉酰基迁移反应","authors":"Yutao Jing, Li Zhang, Li Qiu and Yewen Fang","doi":"10.1039/D5RA01542A","DOIUrl":null,"url":null,"abstract":"<p >Herein, novel SET reduction-based N → C acyl migration protocols for the preparation of functionalized α-amino ketones were successfully developed. In addition to alkyl and silyl radicals, acyl radicals derived from dihydroquinazolinones or acyl oxime acetates could react with enamides to give various 1,4-diketones. These photocatalytic radical addition/acyl migration cascade reactions feature broad substrate scope, good functional group compatibility, and mild reaction conditions.</p>","PeriodicalId":102,"journal":{"name":"RSC Advances","volume":" 15","pages":" 11582-11586"},"PeriodicalIF":4.6000,"publicationDate":"2025-04-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra01542a?page=search","citationCount":"0","resultStr":"{\"title\":\"Modular reductive radical-polar crossover-based acyl migration reactions of N-vinylimides with alkyl, silyl, and acyl radicals†\",\"authors\":\"Yutao Jing, Li Zhang, Li Qiu and Yewen Fang\",\"doi\":\"10.1039/D5RA01542A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Herein, novel SET reduction-based N → C acyl migration protocols for the preparation of functionalized α-amino ketones were successfully developed. In addition to alkyl and silyl radicals, acyl radicals derived from dihydroquinazolinones or acyl oxime acetates could react with enamides to give various 1,4-diketones. These photocatalytic radical addition/acyl migration cascade reactions feature broad substrate scope, good functional group compatibility, and mild reaction conditions.</p>\",\"PeriodicalId\":102,\"journal\":{\"name\":\"RSC Advances\",\"volume\":\" 15\",\"pages\":\" 11582-11586\"},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2025-04-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://pubs.rsc.org/en/content/articlepdf/2025/ra/d5ra01542a?page=search\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"RSC Advances\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra01542a\",\"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":"RSC Advances","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ra/d5ra01542a","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
在此,我们成功开发了基于 SET 还原法的新型 N → C酰基迁移方案,用于制备功能化 α-氨基酮。除烷基和硅基自由基外,来自二氢喹唑啉酮或酰基肟醋酸酯的酰基也能与烯酰胺发生反应,生成各种 1,4-二酮。这些光催化自由基加成/酰基迁移级联反应具有广泛的底物范围、良好的官能团兼容性和温和的反应条件。
Modular reductive radical-polar crossover-based acyl migration reactions of N-vinylimides with alkyl, silyl, and acyl radicals†
Herein, novel SET reduction-based N → C acyl migration protocols for the preparation of functionalized α-amino ketones were successfully developed. In addition to alkyl and silyl radicals, acyl radicals derived from dihydroquinazolinones or acyl oxime acetates could react with enamides to give various 1,4-diketones. These photocatalytic radical addition/acyl migration cascade reactions feature broad substrate scope, good functional group compatibility, and mild reaction conditions.
期刊介绍:
An international, peer-reviewed journal covering all of the chemical sciences, including multidisciplinary and emerging areas. RSC Advances is a gold open access journal allowing researchers free access to research articles, and offering an affordable open access publishing option for authors around the world.