Abstract
AbstractMolecular oxygen‐mediated C−H bond alkylation of cyclic aldimines has been reported, which avoids the use of transition metals and additional oxidants. This method allows straightforward access to a series of cyclic aldimine derivatives through a free radical course. Furthermore, this transformation features mild conditions, excellent yields and good functional group tolerance.
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.
