SYNTHESIS OF 3,4-DIHYDRO-2H-IMIDAZO[2,1-<i>b</i>][1,3,4]THIADIAZINES

Authors

  • А. А. Колодина Rostov State University, Chemical Faculty, Rostov-on-the-Don 344090
  • Н. И. Гапоненко Rostov State University, Chemical Faculty, Rostov-on-the-Don 344090
  • А. В. Лесин Rostov State University, Chemical Faculty, Rostov-on-the-Don 344090

DOI:

https://doi.org/10.1007/7404

Keywords:

N-alkylisatin aminothioimidazole imidazothiadiazine thiobenzyl ether, thiophenacyl ether

Abstract

Thiomethylene-active derivatives of N-imidazolylimines undergo intramolecular cyclization to give 3,4-dihydro-2H-imidazo[2,1-b][1,3,4]thiadiazines. This reaction is a new convenient method for the fusion of a dihydrothiadiazine ring to an imidazole fragment through formation of a C–C bond.

How to Cite
Kolodina, A. A.; Ganonenko, N. I.; Lesin, A. V.  Chem. Heterocycl. Compd. 2007, 43, 1202. [Khim. Geterotsikl. Soedin. 2007, 1415.]

For this article in the English edition see DOI 10.1007/s10593-007-0184-9


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Published

2023-01-30

Issue

No. 9 (2007)

Section

Original Papers