Abstract
Phenyl vinyl sulphone exhibits unusual cathodic behaviour in organic media containing a small excess of a proton donor such as acetic acid or phenol; both the saturated sulphone and an unsaturated dimer are isolated, the formation of which may be explained by hydrogen atom transfer between the organic free radicals formed at the interface.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Journal of the Chemical Society, Chemical Communications
Disclaimer: 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.