Abstract
The Baeyer–Villiger oxidation of apiolaldehyde bearing o-(3-p-anisylisoxazolin-5-yl)methyl substituent proceeds first with the formation of the anticipated phenol. The subsequent oxidation of phenol with destruction of methylenedioxy ring leads to p-quinone derivative which would undergo opening of the benzene ring to finally produce maleic anhydride moiety. The structure of new compounds was proved by X-ray diffraction analysis.
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.
