SOLVOLYSIS OF 2-AMINO-2-THIAZOLINE DERIVATIVES BY ALIPHATIC AMINO ALCOHOLS

Authors

  • А. А. Мандругин M. V. Lomonosov Moscow State University, 119899 Moscow
  • В. М. Федосеев M. V. Lomonosov Moscow State University, 119899 Moscow
  • O. B. Дубовая M. V. Lomonosov Moscow State University, 119899 Moscow
  • А. А. Родюнин M. V. Lomonosov Moscow State University, 119899 Moscow
  • М. И. Семененкo M. V. Lomonosov Moscow State University, 119899 Moscow

Keywords:

N'-(hydroxyalkyl)-2-guanidinoalkanethiols, 2-amino-2-thiazoline derivatives, solvolysis

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.

How to Cite
Mandrugin, A. A.; Fedoseev, V. M.; Dubovaya, O. V.; Rodyunin, A. A.; Semenko, M. N. Chem. Heterocycl. Compd. 2002, 38, 1382. [Khim. Geterotsikl. Soedin. 2002, 1566.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1022190728686

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Published

2002-11-25

Issue

No. 11 (2002)

Section

Original Papers