{"title":"可见光诱导非活化萘的1,4-氨基甲酰吡啶脱芳化反应。","authors":"Cheng-An Jin, Hao Liu, Bo-Wen Xie, Ren-Xiao Liang, Yi-Xia Jia","doi":"10.1039/d5ob00550g","DOIUrl":null,"url":null,"abstract":"<p><p>A visible-light-induced dearomative 1,4-carbamoylpyridinylation of nonactivated naphthalenes is described. The protocol provides rapid access to a series of pyridinylated spiro 1,2-dihydronaphthalenes in moderate yields by using naphthyl-substituted oxamic acids and 4-cyanopyridines as substrates through radical-radical cross-coupling followed by base-mediated alkene tautomerization. In addition, this method enabled late-stage functionalization of several drug derivatives, demonstrating the practical utility of this reaction.</p>","PeriodicalId":96,"journal":{"name":"Organic & Biomolecular Chemistry","volume":" ","pages":""},"PeriodicalIF":2.9000,"publicationDate":"2025-05-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-light-induced dearomative 1,4-carbamoylpyridinylation of nonactivated naphthalenes.\",\"authors\":\"Cheng-An Jin, Hao Liu, Bo-Wen Xie, Ren-Xiao Liang, Yi-Xia Jia\",\"doi\":\"10.1039/d5ob00550g\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A visible-light-induced dearomative 1,4-carbamoylpyridinylation of nonactivated naphthalenes is described. The protocol provides rapid access to a series of pyridinylated spiro 1,2-dihydronaphthalenes in moderate yields by using naphthyl-substituted oxamic acids and 4-cyanopyridines as substrates through radical-radical cross-coupling followed by base-mediated alkene tautomerization. In addition, this method enabled late-stage functionalization of several drug derivatives, demonstrating the practical utility of this reaction.</p>\",\"PeriodicalId\":96,\"journal\":{\"name\":\"Organic & Biomolecular Chemistry\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.9000,\"publicationDate\":\"2025-05-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic & Biomolecular Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1039/d5ob00550g\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic & Biomolecular Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5ob00550g","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Visible-light-induced dearomative 1,4-carbamoylpyridinylation of nonactivated naphthalenes.
A visible-light-induced dearomative 1,4-carbamoylpyridinylation of nonactivated naphthalenes is described. The protocol provides rapid access to a series of pyridinylated spiro 1,2-dihydronaphthalenes in moderate yields by using naphthyl-substituted oxamic acids and 4-cyanopyridines as substrates through radical-radical cross-coupling followed by base-mediated alkene tautomerization. In addition, this method enabled late-stage functionalization of several drug derivatives, demonstrating the practical utility of this reaction.
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.