Abstract
Silyl substituents stabilize ketenes, and permit the preparation of persistent bisketenes, which show characteristic 13C, 17O, and 29Si NMR chemical shifts. The structures and conformations of bisketenes have been examined, as well as their interconversion with cyclobutenediones. A tetraketene has been prepared, and the hydration reactivity of carbon suboxide has been measured. Key words: bisketenes, structures and conformations; cyclobutenedione interconversion.
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.
