Abstract
We report a convenient process for synthesizing indolo-[2,1-a]isoquinoline tetracyclic skeletons in one pot via a low-cost copper-catalyzed tandem amino radical cyclization, in which one C–C bond and one C–N bond are synchronously established.
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.