Chen Yang , Ya-Fei Wan , Tong Sun , Gang Li , Zhang-Jie Shi , Dong Xue
{"title":"Synthesis of carbazoles: light-promoted tandem coupling of nitroarenes with Grignard reagents†","authors":"Chen Yang , Ya-Fei Wan , Tong Sun , Gang Li , Zhang-Jie Shi , Dong Xue","doi":"10.1039/d5qo00019j","DOIUrl":null,"url":null,"abstract":"<div><div>In this study, an efficient method for one-pot synthesis of carbazoles from readily available nitroarenes and Grignard reagents by intermolecular thermal C–N bond coupling followed by a photoinduced aza-6π electrocyclization reaction is reported. The photochemical pathway only requires irradiation of the reaction mixture with purple light (390–395 nm), without any external catalysts and additives, thus providing a novel and step-economic route for the synthesis of carbazoles. Mechanistic studies suggest that nitrosoarene and diarylamine are important intermediates in the reaction process.</div></div>","PeriodicalId":94379,"journal":{"name":"Organic chemistry frontiers : an international journal of organic chemistry","volume":"12 7","pages":"Pages 2165-2172"},"PeriodicalIF":0.0000,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic chemistry frontiers : an international journal of organic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2052412925000683","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/6 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
In this study, an efficient method for one-pot synthesis of carbazoles from readily available nitroarenes and Grignard reagents by intermolecular thermal C–N bond coupling followed by a photoinduced aza-6π electrocyclization reaction is reported. The photochemical pathway only requires irradiation of the reaction mixture with purple light (390–395 nm), without any external catalysts and additives, thus providing a novel and step-economic route for the synthesis of carbazoles. Mechanistic studies suggest that nitrosoarene and diarylamine are important intermediates in the reaction process.