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Polymorphism of heterochromatic regions of flax chromosomes.
The C-banding technique was used to study flax chromosomes (Linum usitatissimum L., 2n = 30). Heterochromatin was located mainly in pericentromeric regions of chromosomes. In spite of small sizeExpand
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 hydrosilaneExpand
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-containingExpand
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 lithiumExpand
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 ofExpand
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 ofExpand
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 hydrogenExpand