Synthesis of 2-(3-hydroxyacetonyl)malonic aldehyde and its derivatives. Their reactions with 5-aminotetrazole

Authors

  • X. P. Сков Hexagon Chemistry Consultants, DK-1460 Copenhagen
  • O. Л. Елисеев N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow
  • М. M. Вартанян N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, 117913 Moscow

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.

How to Cite
Skov, K. R.; Eliseev, O. L.; Vartanyan, M. M. Chem. Heterocycl. Compd. 1997, 33, 703. [Khim. Geterotsikl. Soedin. 1997, 807.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02291803

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Published

1997-06-25

Issue

No. 6 (1997)

Section

Original Papers