Abstract
N‐aryl acrylamides were found to be the more activated Michael acceptor forBaylis–Hillman reaction than acrylamides and N‐alkyl acrylamides. Treatment of N‐aryl acrylamides with aromatic aldehydes in the presence of DABCO (1,4‐diazabicyclo[2·2·2]octane) afforded the desired Baylis–Hillman products, α‐substituted acrylamide derivatives, which have important applications as novel radical polymerization monomers and biologically important reagents.
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.
