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Derivatives of 3-thiocyanophenothiazine Communication 2: Direction of the thiocyanation reaction in 2-chlorophenothiazine

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Bulletin of the Academy of Sciences of the USSR, Division of chemical science Aims and scope

Conclusions

In monosubstitution the thiocyanate group goes to the 7 position of the phenothiazine ring.

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Literature cited

  1. M. V. Rubtsov and A. G. Baichikov, Synthetic Chemical-Pharmaceutical Preparations [in Russian], Meditsina, Moscow (1971), p. 263.

    Google Scholar 

  2. D. Kh. Yarmukhametova, K. Dzhundubaev, B. V. Kudryavtsev, and V. S. Buzlama, Chemistry and Biological Properties of Organophosphorus Derivatives of Phenothiazine [in Russian], Ilim, Frunze (1975).

    Google Scholar 

  3. D. A. Kharkevicha, (ed.), Compilation of Progress in Creation of New Medicinal Media, Meditsina, Moscow (1973), pp. 15–52.

    Google Scholar 

  4. IUPAC Rules of Nomenclature for Chemistry [in Russian], Vol. 2(1), VINITI, Moscow (1979), p. 144.

  5. C. Bodea and M. Terdic, Acad. Rep. Populare Romine, Filiale Cluj, Studii Cerculari Chim.,12, 309–14 (1961).

    Google Scholar 

  6. F. A. Carey and R. J. Sundberg, Advanced Organic Chemistry, part A, Structure and Mechanisms, Plenum Publishing Corp., New York.

  7. E. R. Hester and P. S. Williams, J. Chem. Soc. Perkin Trans.,2,5, 852 (1981).

    Google Scholar 

  8. D. B. Staiger, R. S. Warren, A. P. Zarembo, and E. L. Anderson, J. Heterocycl. Chem.,18, 101 (1981).

    Google Scholar 

  9. G. C. Levy, R. L. Lichter, and G. L. Nelson, Carbon-13 Nuclear Magnetic Resonance Spectroscopy, John Wiley, New York (1980).

    Google Scholar 

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Author information

Authors and Affiliations

  1. A. E. Arbuzov Institute of Organic and Physical Chemistry, Kazan Branch, Academy of Sciences of the USSR, USSR

    A. A. Shtyrlina, D. Kh. Yarmukhametova, K. M. Enikeev, I. É. Ismaev & I. A. Nuretdinov

Authors
  1. A. A. Shtyrlina
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  2. D. Kh. Yarmukhametova
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  3. K. M. Enikeev
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  4. I. É. Ismaev
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  5. I. A. Nuretdinov
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Additional information

Translated from Izvestiya Akademii Nauk SSSR, Seriya Khimicheskaya, No. 10, pp. 2361–2369, October, 1983.

The authors wish to thank A. V. Il'yasov for his participation in the discussion of the results of this investigation.

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Shtyrlina, A.A., Yarmukhametova, D.K., Enikeev, K.M. et al. Derivatives of 3-thiocyanophenothiazine Communication 2: Direction of the thiocyanation reaction in 2-chlorophenothiazine. Russ Chem Bull 32, 2127–2130 (1983). https://doi.org/10.1007/BF00955786

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  • DOI: https://doi.org/10.1007/BF00955786

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