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Correlation of the Homo–Lumo Gap in Furyl and Thienyl Nitrones and Nitroethenes with their Electrochemical Redox Potentials*
Two series of potentially biologically active heteroaryl derivatives of nitrones and nitroethenes have been prepared and studied by cyclic voltammetry and DFT modeling. Satisfactory correlations of
Polymorphism of heterochromatic regions of flax chromosomes.
The intraspecies polymorphism revealed in the chromosomal C-banding pattern makes possible the use of C-bands as chromosome markers in the studies of genetic and genomic polymorphism of this species.
Synthesis and cytotoxic activity of new 2-[(3-aminopropyl)dimethylsilyl]-5-triethylsilylfurans
Highly cytotoxic 3-aminopropyl derivatives of 5-triethylsilyl-2-dimethylsilylfuran (LC501–3 µg ml−1) have been prepared by hydrosilylation of heterocyclic N-allylamines with corresponding hydrosilane
Synthesis, structure and cytotoxic activity of new 1‐[5‐organylsilyl(germyl)‐2‐furyl (thienyl)]nitroethenes
New highly cytotoxic 1-[5-organylsilyl(germyl)-2-furyl(thienyl)]nitroethenes (IC500.3–3 µg ml−1) have been prepared by condensation reaction of corresponding silicon- and germanium-containing
Synthesis, structure and cytotoxic activity of 2‐acetyl‐5‐trimethylsilylthiophene(furan) and their oximes
5-Trimethylsilylderivatives of 2-acetylthiophene and -furan have been regioselectively prepared by a one-pot procedure from the corresponding 2-acetylfuran or 2-acetylthiophene using lithium
Synthesis and cytotoxic activity of 1-{3-[1-(5-organylsilylfuran-2-yl)silinan-1-yl]propyl}amines and some trimethylgermyl analogues.
New highly cytotoxic 1-{3-[1-(5-organylsilyl-furan-2-yl)silinan-1-yl]propyl}amines and some trimethylgermyl analogues (IC50 1-7 μg mL(-1)) have been synthesized by a hydrosilylation reaction of
The title compound, C14H11Cl3N4O2, consists of two planar fragments which are nearly perpendicular to one another. The crystal packing is controlled by intra- and intermolecular C-H...O hydrogen