{"title":"可见光辅助下(苯基)(三氟甲基磺酰基)-λ3-碘烷与烯烃的反应","authors":"A. S. Ganin, M. Yu. Moskalik","doi":"10.1007/s11172-025-4509-6","DOIUrl":null,"url":null,"abstract":"<div><p>Visible light-assisted (<i>λ</i> = 465–470 nm) reactions of (phenyl)(trifluoromethylsulfonylimino)-λ<sup>3</sup>-iodane with alkenes gave products of sulfonamidation and cyclization. Solvent effect on the product composition was revealed. A comparison of the reactions of the title iodane with cyclohexene carried out in the presence of <i>N</i>-halosuccinimides and under blue LED-light-activation conditions (440–450 nm) revealed the differences in triflamidation reaction producing cyclic (aziridine) and linear (halo amides, halo amidines) products. Plausible reaction mechanisms were discussed.</p></div>","PeriodicalId":756,"journal":{"name":"Russian Chemical Bulletin","volume":"74 1","pages":"137 - 142"},"PeriodicalIF":1.7000,"publicationDate":"2025-03-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible light-assisted reactions of (phenyl)(trifluoromethylsulfonylimino)-λ3-iodane with alkenes\",\"authors\":\"A. S. Ganin, M. Yu. Moskalik\",\"doi\":\"10.1007/s11172-025-4509-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Visible light-assisted (<i>λ</i> = 465–470 nm) reactions of (phenyl)(trifluoromethylsulfonylimino)-λ<sup>3</sup>-iodane with alkenes gave products of sulfonamidation and cyclization. Solvent effect on the product composition was revealed. A comparison of the reactions of the title iodane with cyclohexene carried out in the presence of <i>N</i>-halosuccinimides and under blue LED-light-activation conditions (440–450 nm) revealed the differences in triflamidation reaction producing cyclic (aziridine) and linear (halo amides, halo amidines) products. Plausible reaction mechanisms were discussed.</p></div>\",\"PeriodicalId\":756,\"journal\":{\"name\":\"Russian Chemical Bulletin\",\"volume\":\"74 1\",\"pages\":\"137 - 142\"},\"PeriodicalIF\":1.7000,\"publicationDate\":\"2025-03-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Chemical Bulletin\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://link.springer.com/article/10.1007/s11172-025-4509-6\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Chemical Bulletin","FirstCategoryId":"92","ListUrlMain":"https://link.springer.com/article/10.1007/s11172-025-4509-6","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Visible light-assisted reactions of (phenyl)(trifluoromethylsulfonylimino)-λ3-iodane with alkenes
Visible light-assisted (λ = 465–470 nm) reactions of (phenyl)(trifluoromethylsulfonylimino)-λ3-iodane with alkenes gave products of sulfonamidation and cyclization. Solvent effect on the product composition was revealed. A comparison of the reactions of the title iodane with cyclohexene carried out in the presence of N-halosuccinimides and under blue LED-light-activation conditions (440–450 nm) revealed the differences in triflamidation reaction producing cyclic (aziridine) and linear (halo amides, halo amidines) products. Plausible reaction mechanisms were discussed.
期刊介绍:
Publishing nearly 500 original articles a year, by leading Scientists from Russia and throughout the world, Russian Chemical Bulletin is a prominent international journal. The coverage of the journal spans practically all areas of fundamental chemical research and is presented in five sections:
General and Inorganic Chemistry;
Physical Chemistry;
Organic Chemistry;
Organometallic Chemistry;
Chemistry of Natural Compounds and Bioorganic Chemistry.