Abstract
1-Aryl-3-(1-aryl-4-chloro-1H-imidazol-5-yl)prop-2-en-1-ones prepared from 1-aryl-4-chloro-1H-imidazole-5-carbaldehydes and methyl aryl ketones reacted with nitromethane affording 1-aryl-3-(1-aryl-4-chloro-1H-imidazol-5-yl)-4-nitrobutan-1-ones which were reduced with zink in acetic acid to obtain 1-aryl-5-(2-aryl-3,4-dihydro-2H-pyrrol-4-yl)-4-chloro-1H-imidazoles.
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Original Russian Text © O.Ya. Mel’nik, V.A. Chornous, M.V. Vovk, 2015, published in Zhurnal Organicheskoi Khimii, 2015, Vol. 51, No. 2, pp. 250–254.
For communication VIII, see [1].
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Mel’nik, O.Y., Chornous, V.A. & Vovk, M.V. Polyfunctional imidazoles: IX. Synthesis of 1-aryl-5-(2-aryl-3,4-dihydro-2H-pyrrol-4-yl)-4-chloro-1H-imidazoles. Russ J Org Chem 51, 240–244 (2015). https://doi.org/10.1134/S1070428015020189
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DOI: https://doi.org/10.1134/S1070428015020189