Xuemei Zhao , Zhiyuan Tang , Linlin Shi , Yujing Guo , Rene M. Koenigs , Xinqi Hao
{"title":"亚氨基碘烷与硫氧化物的光化学芘转移反应","authors":"Xuemei Zhao , Zhiyuan Tang , Linlin Shi , Yujing Guo , Rene M. Koenigs , Xinqi Hao","doi":"10.1016/j.gresc.2024.05.001","DOIUrl":null,"url":null,"abstract":"<div><div>Nitrene, as an important and intriguing versatile synthon, is widely utilized for the formation of diverse nitrogenous skeletons under thermal or photochemical conditions. Typically, the <em>N</em>-sulfonyl nitrenes could be smoothly generated from iminoiodinanes at relatively low reaction temperatures to generate <em>N</em>-sulfonyl nitrenes. Herein, we described the direct immidation reaction of iminoiodinanes with sulfoxides through a blue-light-induced nitrenes transfer process. This strategy offers an efficient and gentle pathway for directly obtaining sulfoximines within a reaction time of only 10 min. Moreover, the reaction conditions do not necessitate the exclusion of moisture or air, rendering this photocatalytic amination reaction highly practical. A broad range of iminoiodinanes were well tolerated and reacted with sulfoxides smoothly to give the corresponding products in moderate to good yields, which provides a practical and green protocol to access <em>N</em>-sulfonyl architectures.</div></div>","PeriodicalId":12794,"journal":{"name":"Green Synthesis and Catalysis","volume":"7 2","pages":"Pages 211-217"},"PeriodicalIF":0.0000,"publicationDate":"2026-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Photochemical nitrene transfer reactions of iminoiodinanes with sulfoxides\",\"authors\":\"Xuemei Zhao , Zhiyuan Tang , Linlin Shi , Yujing Guo , Rene M. Koenigs , Xinqi Hao\",\"doi\":\"10.1016/j.gresc.2024.05.001\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Nitrene, as an important and intriguing versatile synthon, is widely utilized for the formation of diverse nitrogenous skeletons under thermal or photochemical conditions. Typically, the <em>N</em>-sulfonyl nitrenes could be smoothly generated from iminoiodinanes at relatively low reaction temperatures to generate <em>N</em>-sulfonyl nitrenes. Herein, we described the direct immidation reaction of iminoiodinanes with sulfoxides through a blue-light-induced nitrenes transfer process. This strategy offers an efficient and gentle pathway for directly obtaining sulfoximines within a reaction time of only 10 min. Moreover, the reaction conditions do not necessitate the exclusion of moisture or air, rendering this photocatalytic amination reaction highly practical. A broad range of iminoiodinanes were well tolerated and reacted with sulfoxides smoothly to give the corresponding products in moderate to good yields, which provides a practical and green protocol to access <em>N</em>-sulfonyl architectures.</div></div>\",\"PeriodicalId\":12794,\"journal\":{\"name\":\"Green Synthesis and Catalysis\",\"volume\":\"7 2\",\"pages\":\"Pages 211-217\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2026-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Synthesis and Catalysis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666554924000541\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/5/15 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Green Synthesis and Catalysis","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666554924000541","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/5/15 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
Photochemical nitrene transfer reactions of iminoiodinanes with sulfoxides
Nitrene, as an important and intriguing versatile synthon, is widely utilized for the formation of diverse nitrogenous skeletons under thermal or photochemical conditions. Typically, the N-sulfonyl nitrenes could be smoothly generated from iminoiodinanes at relatively low reaction temperatures to generate N-sulfonyl nitrenes. Herein, we described the direct immidation reaction of iminoiodinanes with sulfoxides through a blue-light-induced nitrenes transfer process. This strategy offers an efficient and gentle pathway for directly obtaining sulfoximines within a reaction time of only 10 min. Moreover, the reaction conditions do not necessitate the exclusion of moisture or air, rendering this photocatalytic amination reaction highly practical. A broad range of iminoiodinanes were well tolerated and reacted with sulfoxides smoothly to give the corresponding products in moderate to good yields, which provides a practical and green protocol to access N-sulfonyl architectures.