Abstract
A versatile and convenient method for synthesis of β-lactams using 3,6-dichlorotetrazine as an acid activator in the ketene–imine cycloaddition is reported. Monocyclic and spirocyclic β-lactams are obtained in good to excellent yields. Easy purification of the products can be performed by aqueous workup and then crystallisation from ethyl acetate.
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.
