Course of bromination of thiazole and 2-methylthiazole

Bromination of thiazole by bromine in the presence of aluminum chloride in neutral solvent or without solvent takes place at the 2-position. Such an orientation contradicts the traditional addition-cleavage mechanism, and agrees with the ylid mechanism of electrophilic substitution. 2-Methylthiazole brominates at the 5-position, and the reaction is impeded in the presence of aluminum chloride; this is due to heterocycle deactivation by complexation with the Lewis acid at the nitrogen atom.Deceased.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 837–840, June, 1986.     

Radical intermediates in the electrochemical reduction of alizarin

Conclusions In the electroreduction of alizarin in an aprotic medium the stepwise formation of the anion-radical and subsequently of the dianion has been observed; under conditions of the prolonged process the anion-radical disproportionates and through intermediate stages of deprotonation and reduction is converted into the stable dianion-radical.Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 5, pp. 983–988, May, 1985.     

IR spectra of selenophenopyrylium salts

On the basis of the IR spectra of 16 alkyl-substituted selenopheno[2,3-c]- and selenopheno-[3,2-c]pyrylium salts and a model calculation of the frequencies and the forms of their normal vibrations, an assignment of the frequencies of the skeletal vibrations of the heterocycles is put forward.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 11, pp. 1495–1497, November, 1973.     

Fluorosulfonyl-containing heterocyclic compounds

Hexafluoroisobutenylidene sulfate is a sulfotrioxidizing agent with respect to various olefins; methylenemethionic acid is formed in the case of ethylene, while the corresponding-sulfones are formed in the case of tetrafluoroethylene and vinylidene fluoride. 2,2-Difluoro-2-hydroxy-ethanesulfonic acid sultone is characterized by a capacity for anionotropic transformations; a number of sulfoacetic acid derivatives were obtained on the basis of this sultone.See [1] for communication III.Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 178–182, February, 1973.