Abstract
Various tosylhydrazones, such as dialkyl and aryl-alkyl tosylhydrazones, were found to react with a peroxysulfur intermediate, which was generated by the reaction of 2-nitrobenzenesulfonyl chloride with superoxide, to be converted into the corresponding carbonyl compounds, in mostly quantitative yields, at −30°C 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.
