Header menu link for other important links
An organophotoredox-catalyzed redox-neutral cascade involving: N -(acyloxy)phthalimides and maleimides
S. Das, S.K. Parida, T. Mandal, S.K. Hota, L. Roy, S. De Sarkar,
Published in Royal Society of Chemistry
Volume: 8
Issue: 10
Pages: 2256 - 2262
An organophotoredox-catalyzed reduction/addition/oxidation cascade of N-protected maleimides and N-(acyloxy)phthalimides is documented. The mild and efficient redox-neutral process involves the hitherto unknown Giese-type addition of aryloxy-alkyl radicals on N-protected maleimides and a successive oxidation allowing an overall Z-alkenylation of the N-substituted pyrrolidine-2,5-dione motif through a formal translocation of the maleimide double bond. © the Partner Organisations.
About the journal
JournalData powered by TypesetOrganic Chemistry Frontiers
PublisherData powered by TypesetRoyal Society of Chemistry