Microwave-assisted Michael reaction between EMME and various amines such as diphenylamine, 4-methyl-N-phenylbenzenamine, N-phenylnaphthalen-1-amine, dihexylamine, diisopropylamine, and 4-nitrobenzenamine were described. Solvent-free conditions on alumina as solid support in the presence of K 2CO3 catalysts gave moderate to good yields (55 - 93%) of diethylmalonate analogues having enamine moieties under focused microwave irradiation.
CITATION STYLE
Kim, K. W., Lee, H. J., Jo, J. I., & Kwon, T. W. (2010). Solvent-free michael addition between EMME and secondary amine under focused microwave irradiation. Bulletin of the Korean Chemical Society, 31(5), 1155–1158. https://doi.org/10.5012/bkcs.2010.31.5.1155
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