Abstract
AbstractIn the presence of Lewis acids, diethyl phosphorochloridite reacts with norbornadiene to afford the tetracyclic phosphinate ester 3. The reaction is believed to involve formation of phosphenium ions stabilized only by alkoxy substituents. The cycloadduct of the reaction was characterized by its spectral data, by single crystal diffraction analysis of the parent acid, and 31P and 27Al nmr experiments.
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.
