Abstract
3,7-Diaminobicyclo[3.3.1]nonanes were synthesized starting from adamantane-2-on. endo,endo-3,7-Diaminobicyclo[3.3.1]nonane was obtained through Schmidt rearrangement of 3,7-bicyclo[3.3.1]nonane dicarboxylic acid. The endo,exo-isomer was synthesized by Schmidt rearrangement of 3-oximinobicyclo[3.3.1]nonane-7-carboxylic acid in acidic media following reduction of oximino group which was unprecedentedly stable in the Schmidt reaction conditions.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
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.