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Mendeleev Communications, 1993, Volume 3, Issue 4, Pages 168–169
DOI: https://doi.org/10.1070/MC1993v003n04ABEH000273
(Mi mendc5316)
 

This article is cited in 10 scientific papers (total in 10 papers)

Ring–Ring Tautomerism of Aldohexose Thiocarbohydrazones

K. N. Zelenina, V. V. Alekseeva, P. B. Terentievb, O. B. Kuznetsovaa, V. V. Lashinb, V. V. Ovcharenkob, V. V. Torocheshnikovb, L. A. Khorseyevaa, A. A. Sorokinc

a S.M. Kirov Military Medical Academy, St. Petersburg, Russian Federation
b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
c All-Russia Scientific Centre of Biologically Active Compounds, Moscow region, Russian Federation
Abstract: Mannose, galactose and glucose thiosemicarbazones, and mannose thiocarbohydrazones exist in DMSO solutions as tautomeric mixtures of pyranose and linear hydrazone forms, but in solutions of galactose and glucose thiocarbohydrazones there are also hexahydro-1,2,4,5-tetrazine-3-thione tautomers.
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Document Type: Article
Language: English


Citation: K. N. Zelenin, V. V. Alekseev, P. B. Terentiev, O. B. Kuznetsova, V. V. Lashin, V. V. Ovcharenko, V. V. Torocheshnikov, L. A. Khorseyeva, A. A. Sorokin, “Ring–Ring Tautomerism of Aldohexose Thiocarbohydrazones”, Mendeleev Commun., 3:4 (1993), 168–169
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  • https://www.mathnet.ru/eng/mendc/v3/i4/p168
  • This publication is cited in the following 10 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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