Abstract
By the ring cleavage of p-nitrophenyloxirane with p-chlorobenzylamine the corresponding chlorobenzyl- and nitrophenyl-substituted aminoethanol was obtained that was brought into reactions of glycosylation, reduction and substitution aimed at the preparation and designing of new structures containing pharmacalogically active functional groups. Among the synthesized compounds a compound is revealed possessing moderately expressed antibacterial and antifungal activity.
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Original Russian Text © I.V. Kulakov, Z.M. Zhambekov, S.D. Fazylov, O.A. Nurkenov, 2008, published in Zhurnal Obshchei Khimii, 2008, Vol. 78, No. 12, pp. 2028–2032.
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Kulakov, I.V., Zhambekov, Z.M., Fazylov, S.D. et al. Synthesis of 2-(4-chlorobenzylamino)-1-(4-nitrophenyl)ethanol and its chemical transformations. Russ J Gen Chem 78, 2374–2378 (2008). https://doi.org/10.1134/S107036320812013X
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DOI: https://doi.org/10.1134/S107036320812013X