Abstract
Treatment of methyl linoleate with 4-phenyl-1,2,4-triazoline-3,5-dione affords 1:1 adducts resulting from ene addition, and 1:2 adducts formed by ene addition followed by Diels Alder cycloaddition. The corresponding reaction of diethyl azodicarboxylate yields predominantly 1:1 ene products.
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