Abstract
The prototropic transformation of O-(N′-methylcarbamidomethyl)-N-carboisopropoxy-N-phenylhydroxylamine in the presence of sodium ethoxide to form isopropyl phenylcarbamate, N-phenyl-N′-methylurea, and glyoxylic acid derivatives was studied. A similar reaction with 2-phenyl-4-methyl-1,2,4-oxadiazine-3,5-dione is accompanied by ring contraction and the formation of 1-phenyl-3-methyl-5-hydroxyhydantoin.
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.
