The reactions of a series of urea- and amide-substituted olefins with Grubbs’ catalysts are presented. Depending on the substrate’s nature, the formation of either cross-metathesis or isomerization products is observed. To favor the cross-metathesis products, the reactions have been carried out using a wide range of experimental conditions. Upon addition of monophenyl phosphoester to these reactions, the isomerization of the olefins is completely suppressed and the cross-metathesis products are obtained in up to 60% yield.
P. Formentín, N. Gimeno, J. H. G. Steinke, R. Vilar
J. Org. Chem. 2005, 70, 8235-8238
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