{"title":"光诱导镍催化的单氟、宝石二氟和三氟甲基系连烯烃的碳卤化反应","authors":"Ruchi Sharma, Naveen Sihag, Poorvi Gupta, Kuntal Manna, M. Ramu Yadav","doi":"10.1039/d5cc01034a","DOIUrl":null,"url":null,"abstract":"Photoexcited nickel-catalyzed carbohalogenation reaction of fluoroalkenes has been demonstrated to afford halofluoroalkyl oxindoles featuring a quaternary center. The broad substrate scope with retention of fluorine atoms followed by efficient synthetic transformations of iodo-gem-difluoroalkyl oxindoles highlight the advantages of this methodology. Additionally, control experiments and DFT calculations have been conducted to illuminate the significance of the triplet-excited state of the nickel catalyst.","PeriodicalId":67,"journal":{"name":"Chemical Communications","volume":"74 1","pages":""},"PeriodicalIF":4.3000,"publicationDate":"2025-04-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photoinduced Ni-Catalyzed Carbohalogenation of mono-Fluoro, gem-Difluoro, and Trifluoromethyl Tethered Alkenes\",\"authors\":\"Ruchi Sharma, Naveen Sihag, Poorvi Gupta, Kuntal Manna, M. Ramu Yadav\",\"doi\":\"10.1039/d5cc01034a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Photoexcited nickel-catalyzed carbohalogenation reaction of fluoroalkenes has been demonstrated to afford halofluoroalkyl oxindoles featuring a quaternary center. The broad substrate scope with retention of fluorine atoms followed by efficient synthetic transformations of iodo-gem-difluoroalkyl oxindoles highlight the advantages of this methodology. Additionally, control experiments and DFT calculations have been conducted to illuminate the significance of the triplet-excited state of the nickel catalyst.\",\"PeriodicalId\":67,\"journal\":{\"name\":\"Chemical Communications\",\"volume\":\"74 1\",\"pages\":\"\"},\"PeriodicalIF\":4.3000,\"publicationDate\":\"2025-04-11\",\"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/d5cc01034a\",\"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/d5cc01034a","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Photoinduced Ni-Catalyzed Carbohalogenation of mono-Fluoro, gem-Difluoro, and Trifluoromethyl Tethered Alkenes
Photoexcited nickel-catalyzed carbohalogenation reaction of fluoroalkenes has been demonstrated to afford halofluoroalkyl oxindoles featuring a quaternary center. The broad substrate scope with retention of fluorine atoms followed by efficient synthetic transformations of iodo-gem-difluoroalkyl oxindoles highlight the advantages of this methodology. Additionally, control experiments and DFT calculations have been conducted to illuminate the significance of the triplet-excited state of the nickel catalyst.
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.