Abstract
AbstractA base‐catalyzed novel [3+2] cycloaddition reaction between arylidene‐1‐phenyl succinimides and alkylidene acenaphthylenones is carried out to access succinimide substituted spiro[acenaphthylenone‐cyclopentane]fused scaffolds with high regio‐ and stereo‐selectivity under mild conditions. The reaction of alkylidene acenaphthylenones with 1,4‐benzoxazinone derivatives under the influence of environmentally benign iodine afforded polyheterocyclic compounds embedded with pyrrole moiety. This metal‐free synthesis is highly efficient and atom economic and the protocol obviates column chromatography. The products are isolated by simple decantation followed by washing with solvent.
Sign-in/Register to access full text options 
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.
