Abstract
Abstract The reaction of p-substituted N-sulfinylanilines with styrene oxide in the presence of tetraethylammonium bromide gave the corresponding 1,2,4,5- and 1,2,4,6-tetraarylpiperazines, whose configurations were established on the basis of the NMR spectral studies. On the other hand, while a similar reaction of p-substituted N-sulfinylphenylhydrazines with the oxide in benzene gave the corresponding diaryl disulfide, diaryl sulfide, and p-substituted biphenyl, the reaction in acetonitrile did not give the biphenyl. The pathways for these reactions are suggested.
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.
