Abstract
3-Amino-5-phenyl-1,3-thiazolidin-2-iminium bromide was synthesized for the first time by reaction of (1,2-dibromoethyl)benzene with thiosemicarbazide hydrochloride. Its condensation with aromatic aldehydes afforded the corresponding Schiff bases. The structure of the isolated compounds was confirmed by 1H and 13C NMR spectroscopy.
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Duruskari, G.S., Asgarova, A.R., Aliyeva, K.N. et al. Condensation Products of Aldehydes with Phenylthiazolidine Obtained from (1,2-Dibromoethyl)benzene. Russ J Org Chem 56, 712–715 (2020). https://doi.org/10.1134/S1070428020040223
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DOI: https://doi.org/10.1134/S1070428020040223