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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.
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
Linking options:
https://www.mathnet.ru/eng/mendc5316 https://www.mathnet.ru/eng/mendc/v3/i4/p168
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