The carbonylation at the benzyl C-Hal bonds (Hal = F, Cl) of a number of polyfluorinated alkylbenzenes and benzocycloalkenes using carbon monoxide in the presence of SbF is described. The reaction provided the corresponding -arylcarboxylic acids or their methyl esters following aqueous or methanol treatment. The products of double carbonylation were obtained from bis(chloromethyl)tetrafluorobenzenes and benzal fluorides.
View Article and Find Full Text PDFO-centered tetranuclear vanadium selenoiodide [VOSeI] (1) was synthesized by an ampoule method from the elements with addition of water. Its X-ray crystal structure (space group 2/, = 21.146(2) Å, = 5.
View Article and Find Full Text PDFThe biologically active compound 3-aminopropylsilatrane (a compound with a pentacoordinated silicon atom) underwent an aza-Michael reaction with various acrylates and other Michael acceptors. Depending on the molar ratio, the reaction yielded Michael mono- or diadducts (11 examples) containing functional groups (silatranyl, carbonyl, nitrile, amino, etc.).
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