Condensed heterocycles. 41. Mass spectrometric study of selenol(mercapto)aldimines of benzo[b]thiophene and their S,Se-alkyl derivatives |
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Authors: | B. M. Zolotarev V. P. Litvinov Ya. L. Gol'dfarb V. Yu. Mortikov |
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Affiliation: | (1) N. D. Zelinskii Institute of Organic Chemistry, Academy of Sciences of the USSR, 117913 Moscow |
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Abstract: | The production of imines of 3-selenol(mercapto)-2-benzo[b]thiophenaldehyde and 2-selenol(mercapto)-3-benzo[b]thiophenaldehyde and their S,Se-alkyl derivatives under electron impact was studied. The main distinctions of the decomposition of the molecular ions of selenium-containing compounds from their sulfur analogs, due to the greater strength of the C-S bond in comparison with the C-Se bond, were demonstrated. The different behavior of isomeric 3- and 2-mercaptoaldimines of benzo[b]thiophene was detected.For communication 40, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1057–1061, August, 1984. |
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