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pubmed-article:17602591pubmed:abstractTextReaction of 2-substituted dienamides with catalytic amounts of copper halide/tripyridylamine (TPA) furnishes either 5-exo or 6-endo products with the outcome dependent upon the radical initiating unit. Reaction of 3-substituted dienamides produces beta-lactams via a 4-exo cyclization with termination of the reaction occurring via either halogen atom transfer, trapping with oxygen, elimination, or radical-radical coupling depending upon the diene.lld:pubmed
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pubmed-article:17602591pubmed:articleTitleRegiochemistry of copper(I)-mediated cyclization reactions of halo-dienamides.lld:pubmed
pubmed-article:17602591pubmed:affiliationDepartment of Chemistry, University of Warwick, Coventry, West Midlands, U.K. msrir@csv.warwick.ac.uklld:pubmed
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