Chen Yang , Ya-Fei Wan , Tong Sun , Gang Li , Zhang-Jie Shi , Dong Xue
{"title":"咔唑的合成:硝基芳烃与格氏试剂的光催化串联偶联","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":"{\"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\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","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":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Synthesis of carbazoles: light-promoted tandem coupling of nitroarenes with Grignard reagents†
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.