X-ray structural insights and computational analysis of the compound 5-ethyl-4-[(4-morpholino-benzylidene)amino]-2,4-di-hydro-3<i>H</i>-1,2,4-triazole-3-thione. [PDF]
Nizamuddin S +5 more
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Triazole-imidazo[1,2-<i>b</i>]pyrazoles Able to Counteract Melanoma Cell Survival Without Compromising the Viability of Healthy Keratinocytes. [PDF]
Brullo C +8 more
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7-Methoxybenzofuran-triazole tethered <i>N</i>-phenylacetamides as a promising class of tyrosinase inhibitors: synthesis, biological evaluation and computational analyses against fungal and human tyrosinases. [PDF]
Mushtaq A +5 more
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Bivalent transition metal complexes of triazole pyridine Schiff base with theoretical and biological investigations. [PDF]
Mannaa AH +4 more
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New 1,2,4-Triazole Derivatives with a <i>N</i>-Mannich Base Structure Based on a 4,6-Dimethylpyridine Scaffold as Anticancer Agents: Design, Synthesis, Biological Evaluation, and Molecular Modeling. [PDF]
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Alkylation of 1,2,4-triazole-3-thiols with haloalkanoic acid esters
Russian Journal of Organic Chemistry, 2017Alkylation of 4,5-disubstituted 4H-1,2,4-triazole-3-thiols with methyl chloroformate and ethyl chloroacetate chemoselectively afforded the corresponding S-alkyl derivatives, whereas the alkylation of 5-benzyl-4-phenyl-4H-1,2,4-triazole-3-thiol with methyl 3-bromopropanoate gave an inseparable mixture of S- and N-alkylation products. Hydrazinolysis of S-
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Synthesis of 1,2,4-triazole-3-thiols and their S-substituted derivatives
Russian Journal of Organic Chemistry, 2010New 1,2,4-triazole-3-thiols were synthesized by reactions of the corresponding carboxylic acid hydrazides with isothiocyanates and subsequent cyclization of intermediate 1,4-substituted thiosemicarbazides. Alkylation of 1,2,4-triazole-3-thiols with benzyl chlorides and bromacetophenones gave only S-substituted derivatives.
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Oxidation of 4-amino-5-aryl-4H-1,2,4-triazole-3-thiols
Russian Journal of Organic Chemistry, 2011A simple and efficient method for the preparation of triazolesulfonic acids (II) is presented.
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Synthesis and antimicrobial activity of new 1,2,4-triazole-3-thiol metronidazole derivatives
Monatshefte für Chemie - Chemical Monthly, 2010New 1,2,4-triazole-3-thiol metronidazole derivatives have been synthesized by treating 1,2,4-triazole-3-thiols with metronidazole tosylate (toluene-4-sulfonic acid 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl ester) in DMF and in the presence of potassium carbonate as a base.
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