Palladium-catalyzed C-H alkenylation of C-aryl nitrones

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Abstract

Palladium-catalyzed C-H alkenylation of C-aryl N-t-butyl nitrones with ethyl acrylate produced ortho-alkenylated benzamide derivatives via isomerization of the nitrone moiety. The use of 1,1,1,3,3,3-hexafluoro-2-propanol/acetic acid as a solvent resulted in effective C-H alkenylation, while competitive 1,3-dipolar cycloaddition was completely suppressed.

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Hasegawa, M., Nomoto, A., Suga, T., Soeta, T., & Ukaji, Y. (2017). Palladium-catalyzed C-H alkenylation of C-aryl nitrones. Chemistry Letters, 46(1), 45–47. https://doi.org/10.1246/cl.160821

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