Abstract
AbstractSelenium dioxide is traditionally regarded as an oxidant and rather as a selenium source for making organseliums. Herein, we developed a new selenation method by using selenium dioxide instead of commonly used selenium powder or diselenides to generate Se‐substituted imidazoheterocycle and aniline compounds. Furthermore, sodium arenesulfinates were selected as coupling partners instead of traditional aromatic halides. All reactions give desired products in moderate to excellent yields under mild conditions.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
