Abstract
2-(3-Hydroxyacetonyl)malonic aldehyde and its derivatives were prepared for the first time by the hydrolysis of 2-substituted 2,5-dimethoxy-4-formyltetrahydrofuranes. Their interaction with 5-aminotetrazole gave functionally substituted 6-tetrazolo[1,5-a]pyrimidines.
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References
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Additional information
N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 117913. Hexagon Chemistry Consultants, DK-1460 Copenhagen. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, 807–810, June, 1997.
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Skov, K.R., Eliseev, O.L. & Vartanyan, M.M. Synthesis of 2-(3-hydroxyacetonyl)malonic aldehyde and its derivatives. Their reactions with 5-aminotetrazole. Chem Heterocycl Compd 33, 703–706 (1997). https://doi.org/10.1007/BF02291803
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DOI: https://doi.org/10.1007/BF02291803