Abstract
Microwave irradiation of three component reaction of dimedone, appropriate aromatic aldehydes and amino alcohols in a stoichiometrical ratio 2:1:1 for few minutes afforded the formation of a stable fused three membered ring of the corresponding 3,6,6-tetramethyl-2,3,4,5,6,7,8,9,10-decahydroacridine-1,8-dione derivatives in an excellent yield (80–91%). The structure of all products has been characterized by X-ray crystal structural analyses, 13C NMR, 1H NMR, IR and mass spectrum analyses.
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.
