{"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":"Chandra Volla, Kuntal Pal, Om Prakash Dash","doi":"10.1039/d4cc06346e","DOIUrl":null,"url":null,"abstract":"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.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"12 1","pages":""},"PeriodicalIF":4.3000,"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\":\"Chandra Volla, Kuntal Pal, Om Prakash Dash\",\"doi\":\"10.1039/d4cc06346e\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"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.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"12 1\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"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://doi.org/10.1039/d4cc06346e\",\"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://doi.org/10.1039/d4cc06346e","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:
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