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Research on riboflavin analogs

VIII. 7-Trifluoromethyl-8-chloroisoalloxazines

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

A number of 7-trifluoromethyl-8-chloro-10-R-isoalloxazines (where R=H, CH3, CH2CH2OH, ribityl, galactyl, sorbityl, and rhamnityl) and 7-trifluoromethyl- 8- (β-hydroxyethyl) aminoisoalloxazines with substituents such as ribityl and β-hydroxyethyl in the 10 position were synthesized.

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Literature cited

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Authors and Affiliations

  1. S. M. Kirov Ural Polytechnic Institute, Sverdlovsk

    N. A. Plashkina, V. I. Troitskaya, Z. V. Pushkareva & T. P. Ryapasova

  2. Institute of Organic Chemistry, Academy of Sciences of the Ukrainina SSR, Kiev

    N. A. Plashkina, V. I. Troitskaya, Z. V. Pushkareva & T. P. Ryapasova

Authors
  1. N. A. Plashkina
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  2. V. I. Troitskaya
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  3. Z. V. Pushkareva
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  4. T. P. Ryapasova
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Additional information

See [1] for communication VII.

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1136–1139, August, 1976.

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Plashkina, N.A., Troitskaya, V.I., Pushkareva, Z.V. et al. Research on riboflavin analogs. Chem Heterocycl Compd 12, 938–941 (1976). https://doi.org/10.1007/BF00510121

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  • DOI: https://doi.org/10.1007/BF00510121

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