{"title":"通过 PCET 形成酰胺基,利用镍光氧催化酰胺芳基化反应","authors":"Sodai Nishino, Takuya Kurahashi","doi":"10.1093/chemle/upae088","DOIUrl":null,"url":null,"abstract":"Herein, we report the N-arylation of amides based on the formation of N-centered amidyl radicals via proton-coupled electron transfer (PCET) using a nickel–photoredox dual catalyst. The reaction achieved arylation of sterically hindered linear secondary amides under mild conditions. Control experiments with radical inhibitors suggested the formation of amidyl radicals via the PCET mechanism.","PeriodicalId":9862,"journal":{"name":"Chemistry Letters","volume":null,"pages":null},"PeriodicalIF":1.4000,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Ni-photoredox-catalyzed amide arylation reaction using amidyl radical formation via PCET\",\"authors\":\"Sodai Nishino, Takuya Kurahashi\",\"doi\":\"10.1093/chemle/upae088\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Herein, we report the N-arylation of amides based on the formation of N-centered amidyl radicals via proton-coupled electron transfer (PCET) using a nickel–photoredox dual catalyst. The reaction achieved arylation of sterically hindered linear secondary amides under mild conditions. Control experiments with radical inhibitors suggested the formation of amidyl radicals via the PCET mechanism.\",\"PeriodicalId\":9862,\"journal\":{\"name\":\"Chemistry Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.4000,\"publicationDate\":\"2024-05-30\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemistry Letters\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1093/chemle/upae088\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemistry Letters","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1093/chemle/upae088","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Ni-photoredox-catalyzed amide arylation reaction using amidyl radical formation via PCET
Herein, we report the N-arylation of amides based on the formation of N-centered amidyl radicals via proton-coupled electron transfer (PCET) using a nickel–photoredox dual catalyst. The reaction achieved arylation of sterically hindered linear secondary amides under mild conditions. Control experiments with radical inhibitors suggested the formation of amidyl radicals via the PCET mechanism.