Effect of phase composition of palladium-ruthenium membrane catalyst on selectivity of dehydrolinalool hydrogenation

Conclusions When the hydrogenation of dehydrolinalool to linalool is run on a Pd alloy containing 6 wt.% of Ru, which is lean in the -hydrogen phase, the selectivity is much greater than when the amount of the -hydrogen phase is greater. A high selectivity of the hydrogenation is achieved by reducing to a definite limit the amount of hydrogen in the membrane catalyst without using inhibitors of the side reactions, which can contaminate the hydrogenation products.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 4, pp. 926–928, April, 1984.     

Basicities of phosphinylalkylamines in water and ethanol

Conclusions The pK_a values of various phosphinylalkylamines in water and ethanol were determined. The inductive effect of phosphinyl groups on the basicities of the investigated amines was demonstrated. The inductive constants of a series of substituents were estimated.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 6, pp. 1265–1267, June, 1982.     

1,4 Addition to a perfluorinated cross-conjugated triene

Conclusions Perfluoro-(2-isobutenyl-1,1,4,4-tetramethyl-1,3-butadiene) yields 1,4 addition products both in nucleophilic addition and in radical chlorination.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 1061–1064, May, 1979.     

Reactions of 4-(o-carboranyl)pyrylium salts with nucleophilic agents. Synthesis of nitrogen heterocycles with an o-carboranyl substituent

Nitrogen heterocycles, viz., pyridines, pyridinium salts, diazepine, and pyrazoles, with an o-carboranyl substituent were obtained by reaction of 4-(o-carboranyl)-pyrylium perchlorates with nitrogen-containig nucleophilic agents, viz., ammonia, primary amines, hydrazine, and phenylhydrazine. Opening of the pyrylium ring without involvement of the carborane ring occurs under the influence of bases.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 4, pp. 454–458, April, 1981.     

NMR spectra and structure of phospeorylated isothiocyanates

Conclusions The chlorides of dialkyl- and alkylenephosphorous acids react with trimethylsilyl isothiocyanate to give the isothiocyanates of the corresponding phosphorous acids. The reaction goes stereospecifically with a retention of the configuration at the phosphorus atom.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 1, pp. 1380–1383, June, 1976.