Abstract
Nucleophilic substitution of the nitro group in a model representative of N-aminopyrazoles, 1-amino-3,4-dinitropyrazole, has been studied for the first time. The compound was shown to undergo nucleophilic substitution with S-nucleophiles. The reaction was effected with regioselective substitution of the nitro group at position 3 and in good yields.
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.