Abstract
Reaction of erysodienol (4) with methyl iodide afforded the corresponding dibenzazonine (7), whose structure was confirmed by identification with the authentic specimen, prepared by N-methylation of a known secondary amine (1). On the other hand, erysodienone methiodide (6), synthesized by N-methylation of erysodienone (3), was treated with alkali reagents in methanol and ethanol to yield dibenzazonines (8 and 9), which have newly formed methoxyl and ethoxyl groups at C5-position in dibenzazonine skeleton.
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.
