Abstract
Veratraldehyde was condensed with methyl 2-chloropropanoate to give a glycidic ester. This was hydrolyzed with aqueous sodium hydroxide and the resulting sodium salt was treated with lead(IV) tetraacetate to give 1-acetoxy-1-(3, 4-dimethoxyphenyl)propan-2-one (13). Condensation of 13 with dimethyl malonate, followed by acidic hydrolysis and sodium borohydride reduction afforded (2R*, 3S*, 4R*)-4-(3, 4-dimethoxyphenyl)-2-methoxycarbonyl-3-methyl-4-butanolide (7a). The γ-lactone 7a was then converted into 5'-demethoxyporosin (10) by means of a series of reactions : Michael reaction with methyl vinyl ketone, elimination of the methoxycarbonyl group, acetalization, allylation, deacetalization, and intramolecular aldol reaction. Introduction of a hydroxyl group at the C-5' position in 10, followed by methylation with diazomethane afforded racemic porosin. The synthetic porosin was further converted into 5-demethoxymegaphone acetate.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: 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.