Abstract
ω-[(4Z)-2-Aryl-4-arylmethylidene-5-oxo-4,5-dihydro-1H-imidazol-1-yl]alkanoic acids were synthesized by reaction of N-substituted α,β-dehydropeptides with chloro(trimethyl)silane or 1,1,1,3,3,3-hexamethyldisilazane. Both initial peptides and (4H)-imidazol-5-one derivatives based thereon were tested for anticholinesterase activity.
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Original Russian Text © V.O. Topuzyan, V.M. Kazoyan, R.A. Tamazyan, A.G. Aivazyan, L.Kh. Galstyan, 2018, published in Zhurnal Organicheskoi Khimii, 2018, Vol. 54, No. 9, pp. 1355–1363.
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Topuzyan, V.O., Kazoyan, V.M., Tamazyan, R.A. et al. Synthesis and Anticholinesterase Activity of [(4Z)-2-Aryl-4-(arylmethylidene)-5-oxo-4,5-dihydro-1H-imidazol-1-yl]alkanoic Acids. Russ J Org Chem 54, 1369–1377 (2018). https://doi.org/10.1134/S1070428018090178
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DOI: https://doi.org/10.1134/S1070428018090178