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Photochemical nitrene transfer reactions of iminoiodinanes with sulfoxides

Title data

Zhao, Xuemei ; Tang, Zhiyuan ; Shi, Linlin ; Guo, Yujing ; Koenigs, Rene M. ; Hao, Xinqi:
Photochemical nitrene transfer reactions of iminoiodinanes with sulfoxides.
In: Green Synthesis and Catalysis. (2024) .
ISSN 2666-5549
DOI: https://doi.org/10.1016/j.gresc.2024.05.001

Abstract in another language

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.

Further data

Item Type: Article in a journal
Refereed: Yes
Keywords: Nitrene transfer; Photocatalysis; Amination reaction; N-sulfonyl architectures
Institutions of the University: Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry
Result of work at the UBT: No
DDC Subjects: 500 Science > 540 Chemistry
Date Deposited: 28 Mar 2025 09:09
Last Modified: 28 Mar 2025 09:09
URI: https://eref.uni-bayreuth.de/id/eprint/93030