Zobrazeno 1 - 10
of 81
pro vyhledávání: '"B. Modzelewska-Banachiewicz"'
The 1H, 13C and 15N NMR study on 5-carboxymethyl-1,2,4-triazole and 5-oxo-1,2,4-triazine derivatives
Publikováno v:
Journal of Molecular Structure. 562:167-175
The 5-carboxymethyl-1,2,4-triazole ( 1 , 2 , 3 ) and 5-oxo-1,2,4-triazine ( 4 , 5 , 6 ) derivatives were examined in solution by the 1 H, 13 C and 15 N NMR including g -HSQC, g -HMBC 2D techniques and in the solid phase by 13 C CPMAS NMR. Molecular m
Publikováno v:
ChemInform. 30
In this study, the biological activity of the 5-oxo-1,2,4-triazine derivatives 12-17 obtained in a reaction of N3-substituted amidrazones 1-6 with dimethyl acethylenedicarboxylate (DMAD) has been examined.
Publikováno v:
ChemInform. 30
Publikováno v:
Scopus-Elsevier
The physicochemical properties of biogenic monoamines, their polar character, lability and trace amounts found in the biological material create great analytical difficulties in their identification and separation. The selective chromatographic separ
Publikováno v:
Polish journal of veterinary sciences. 9(1)
Successful results of earlier studies on testing the immune-modulating and anti-microbial properties of 1,2,4-triasole derivative as well as benefitial application of natural bio-stimulators in animal's prophylaxis and treatment inspired us to undert
Publikováno v:
Annales Universitatis Mariae Curie-Sklodowska. Sectio D: Medicina. 55
Publikováno v:
Acta poloniae pharmaceutica. 57(3)
Synthesis of some new 1,2,4-triazole and 1,3,4-thiadiazole derivatives via the condensation of N'-substituted amidrazones and p-phenylenediisothiocyanate (PPD) is presented. The reaction conditions are discussed. Results of a preliminary pharmacologi
Publikováno v:
Die Pharmazie. 54(8)
The synthesis of 3,4-disubstituted 5-arylsulphonylamine-1,2,4-triazoles is described. The antimicrobial activities of the compounds were investigated as well as their acute toxicity.
Publikováno v:
Die Pharmazie. 54(7)
In this study, the biological activity of the 5-oxo-1,2,4-triazine derivatives 12-17 obtained in a reaction of N3-substituted amidrazones 1-6 with dimethyl acethylenedicarboxylate (DMAD) has been examined.
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