Abstract
An efficient regioselective copper-catalyzed strategy for the synthesis of 1,2,3-triazoles from N-tosylhydrazones and azides has been reported. This transformation opened a new route to synthesize 1,2,3-triazoles which is a common structural motif in natural products and pharmaceuticals. The reactions were smoothly under the optimized conditions and provided the desired product 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.