Kuntal Pal , Om Prakash Dash , Chandra M. R. Volla
{"title":"铑/硒双催化从n -磺酰基-1,2,3-三唑中获得2-氨基吡咯","authors":"Kuntal Pal , Om Prakash Dash , Chandra M. R. Volla","doi":"10.1039/d4cc06346e","DOIUrl":null,"url":null,"abstract":"<div><div>Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from <em>N</em>-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(<span>ii</span>)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.</div></div>","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"61 19","pages":"Pages 3872-3875"},"PeriodicalIF":4.2000,"publicationDate":"2025-01-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles†\",\"authors\":\"Kuntal Pal , Om Prakash Dash , Chandra M. R. Volla\",\"doi\":\"10.1039/d4cc06346e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from <em>N</em>-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(<span>ii</span>)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.</div></div>\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"61 19\",\"pages\":\"Pages 3872-3875\"},\"PeriodicalIF\":4.2000,\"publicationDate\":\"2025-01-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chemical Communications\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1359734525002617\",\"RegionNum\":2,\"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":"Chemical Communications","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1359734525002617","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Rhodium/selenium dual catalysis for accessing 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles†
Herein, we report a novel rhodium/selenium dual catalytic process for the synthesis of 2-aminopyrroles from N-sulfonyl-1,2,3-triazoles. The proposed cooperative catalytic mechanism involves Rh(ii)-catalyzed formation of Rh-azavinyl carbene from triazole, followed by selenium-catalyzed generation of ylide, which subsequently undergoes annulation with another Rh-azavinyl carbene. The simple and mild dual catalytic strategy accommodates a variety of electron-withdrawing and electron-donating functional groups, affording various 2-aminopyrrole derivatives in moderate to good yields.
期刊介绍:
ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.