Abstract
Reactions of alkyl acetoacetates, aromatic aldehydes, ammonium acetate, and 1,3-cyclohexanedione afford alkyl 4-aryl-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylates. The structure of compounds obtained was established with the help of IR, 1H NMR, and mass spectra and by X-ray diffraction analysis.
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Original English Text © V.L. Gein, M.I. Kazantseva, L.F. Gein, P.A. Slepukhin, 2014, published in Zhurnal Organicheskoi Khimii, 2014, Vol. 50, No. 2, pp. 247–250.
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Gein, V.L., Kazantseva, M.I., Gein, L.F. et al. Synthesis of alkyl 4-aryl-2-methyl-5-oxo-1,4,5,6,7,8-hexahydroquinoline-3-carboxylates. Russ J Org Chem 50, 240–243 (2014). https://doi.org/10.1134/S107042801402016X
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DOI: https://doi.org/10.1134/S107042801402016X