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Solvolysis of 2-Amino-2-thiazoline Derivatives by Aliphatic Amino Alcohols

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The opening of the thiazoline ring upon the action of amino alcohols was studied. The effects of the reagent ratio and structures of the heterocycles and amino alcohols on aminolysis were investigated. A new method was developed for the preparative synthesis of a series of N'-(hydroxyalkyl)-2-guanidinoalkanethiols.

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REFERENCES

  1. V. G. Vladimirov, I. I. Krasil′nikov, and O. V. Arapov, Radioprotectors: Structure and Function [in Russian], Naukova Dumka, Kiev (1989).

    Google Scholar 

  2. F. M. Fedoseev, Thiazolines and Thiazines - A New type of Radioprotective Compounds. Questions in Modern Radiation Pharmacology [in Russian], Nauka, Moscow (1980), p. 10.

    Google Scholar 

  3. G. Hendrik and F. Atkinson, J. Med. Chem., 9, 558 (1966).

    Google Scholar 

  4. A. A. Mandrugin, V. M. Fedoseev, M. N. Semenenko, and S. M. Khomutov, Khim. Geterotsikl. Soedin., 1550 (2000).

  5. A. A. Mandrugin, V. M. Fedoseev, S. M. Khomutov, A. A. Rodyunin, and Yu. A. Leshchev, Khim. Geterotsikl. Soedin., 1572 (1987).

  6. N. M. Turkevich and B. I. Shvydkii, Ukr. Khim. Zh., 18, 513 (1952).

    Google Scholar 

  7. W. O. Foye, T. Mickels, R. N. Duval, and T. R. Marshall, J. Med. Chem., 6, 509 (1963).

    Google Scholar 

  8. E. D. Manolov, Farmatsiya, No. 15, 271 (1965).

    Google Scholar 

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Mandrugin, A.A., Fedoseev, V.M., Dubovaya, O.V. et al. Solvolysis of 2-Amino-2-thiazoline Derivatives by Aliphatic Amino Alcohols. Chemistry of Heterocyclic Compounds 38, 1382–1388 (2002). https://doi.org/10.1023/A:1022190728686

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  • DOI: https://doi.org/10.1023/A:1022190728686

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