Abstract
Radical cyclizations to dicyanocyclopropanes provide cyclic enaminonitriles by a series of radical reactions that features radical cyclization to a nitrile and cyclopropane cleavage. The direction of cyclopropane cleavage - and hence the ring size of the final product - depends on the nature of the ring formed in the initial cyclization to the nitrile.
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.
