亚氨基碘烷与硫氧化物的光化学芘转移反应

Green Synthesis and Catalysis Pub Date : 2026-04-01 Epub Date: 2024-05-15 DOI:10.1016/j.gresc.2024.05.001
Xuemei Zhao , Zhiyuan Tang , Linlin Shi , Yujing Guo , Rene M. Koenigs , Xinqi Hao
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引用次数: 0

摘要

硝基烯是一种重要而有趣的多用途合成物,被广泛用于在热或光化学条件下形成各种含氮骨架。通常,在较低的反应温度下,亚胺碘胺可以顺利地生成n -磺酰基亚硝基。在此,我们描述了通过蓝光诱导的亚硝基转移过程,亚胺碘胺与亚砜的直接模拟反应。该策略为直接获得亚砜亚胺提供了一种有效而温和的途径,反应时间仅为10分钟。此外,反应条件不需要排除水分或空气,使得这种光催化胺化反应非常实用。广泛的亚胺碘胺具有良好的耐受性,并能与亚砜顺利反应,以中高收率得到相应的产物,这为获得n -磺酰基结构提供了一种实用的绿色方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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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.
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