Abstract
3-Phenyl-1-(thiophen-2-yl)prop-2-en-1-one obtained by Claisen-Schmidt condensation of 2-acetyl thiophene with benzaldehyde was converted into 2,3-dibromo-3-phenyl-1-(thiophen-2-yl)propan-1-one, which on treatment with various thiosemicarbazides in the presence of triethylamine in absolute ethanol, yielded the corresponding hydroxy pyrazolines 3a-h. All the compounds were characterized by IR, 1H NMR, and 13C NMR spectra. Copyright © Taylor & Francis Group, LLC.
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Parveen, H., Iqbal, P. F., & Azam, A. (2008). Synthesis and characterization of a new series of hydroxy pyrazolines. Synthetic Communications, 38(22), 3973–3983. https://doi.org/10.1080/00397910802241407
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