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Pharmaceutical Chemistry Journal

, Volume 14, Issue 3, pp 162–169 | Cite as

Antimicrobial activity of some acyl halide arylhydrazones and carboxylic acid arylhydrazides

  • Zh. V. Molodykh
  • B. I. Buzykin
  • M. A. Kudrina
  • L. P. Sysoeva
  • N. G. Gazetdinova
  • I. D. Neklesova
  • Yu. P. Kitaev
Article

Keywords

Organic Chemistry Antimicrobial Activity Carboxylic Acid Halide Acyl Halide 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

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Literature cited

  1. 1.
    Yu. P. Kitaev and B. I. Buzykin, Hydrazones [in Russian], Moscow (1974), pp. 151–218.Google Scholar
  2. 2.
    S. D. Folz, U. S. Patent No. 3721740; Ref. Zh. Khim., No. 3, N266 (1974).Google Scholar
  3. 3.
    Zh. V. Molodykh, A. N. Lisenkova, B. I. Buzykin, et al., Khim.-Farm. Zh., No. 1, 81 (1977).Google Scholar
  4. 4.
    J. E. Moore, U. S. Patent No. 3867449; Ref. Zh. Khim., 240512 (1975).Google Scholar
  5. 5.
    G. Kaugars and E. G. H. Gemrich, U. S. Patent No. 3879543; Ref. Zh. Khim., 50396 (1976).Google Scholar
  6. 6.
    T. Noguchi, T. Hosotsuji, H. Ishikawa, et al., Japanese Patent No. 43111; Ref. Zh. Khim., 18N497 (1972).Google Scholar
  7. 7.
    M. O. Lozinskii, M. N. Rotmistrov, S. N. Kukota, et al., in: Physiologically Active Substances [in Russian]., Vol. 2, Kiev (1969), pp. 195–198.Google Scholar
  8. 8.
    A. I. Dychenko, E. F. Granin, L. P. Charuiskaya, et al., in: Physiologically Active Substances [in Russian], Vol. 9, Kiev (1977), pp. 54–56.Google Scholar
  9. 9.
    A. E. Smith, G. E. O'Brien, and A. Bernmann, U. S. Patent No, 2758051; Chem. Abstr.,51, 1524b (1957).Google Scholar
  10. 10.
    Y. Usui and Ch. Matsumura, Yakugaku Zasshi,87, 38 (1967); Chem. Abstr.,67, 11452 (1967).Google Scholar
  11. 11.
    Y. Usui and Ch. Matsumura, Yakugaku Zasshi,87, 43 (1967); Chem. Abstr.,67, 32382a (1967).Google Scholar
  12. 12.
    P. E. Frohberger, E. Urbschat, D. Mayer, et al., German Patent No. 2223936; Chem. Abstr.,80, 70557 (1974).Google Scholar
  13. 13.
    T. Taniguchi, Y. Yasuda, A. Nakada, et al., Japanese Patent No. 4911061; Ref. Zh. Khim., 23N628 (1974).Google Scholar
  14. 14.
    Dutch Patent No. 145435; Ref. Zh. Khim., 90354 (1976).Google Scholar
  15. 15.
    S. N. Milovanova and Z. G. Stepanishcheva, in: G. N. Pershin (editor), Methods of Experimental Chemotherapy [in Russian], Moscow (1971), 2nd edn., pp. 318–320.Google Scholar
  16. 16.
    S. N. Milovanova, in: G. N. Pershin (editor), Methods of Experimental Chemotherapy [in Russian], Moscow (1971), 2nd edn., pp. 104–106.Google Scholar
  17. 17.
    M. L. Belen'kii, Elements of the Quantitative Evaluation of Pharmacological Effect [in Russian], Leningrad (1963), 2nd edn.Google Scholar
  18. 19.
    Yu. P. Kitaev, B. I. Buzykin, and L. P. Sysoeva, Zh. Org. Khim.,8, 515 (1972).Google Scholar

Copyright information

© Plenum Publishing Corporation 1981

Authors and Affiliations

  • Zh. V. Molodykh
    • 1
  • B. I. Buzykin
    • 1
  • M. A. Kudrina
    • 1
  • L. P. Sysoeva
    • 1
  • N. G. Gazetdinova
    • 1
  • I. D. Neklesova
    • 1
  • Yu. P. Kitaev
    • 1
  1. 1.A. E. Arbuzov Institute of Organic and Physical ChemistryAcademy of Sciences of the USSRKazan'

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