New 2-hydrazonophenylthioacetamides intermediates in the synthesis of 6-acylamino-3,6-dihydro-2h-1,3,4-thiadiazines

Article abstract of DOI:10.1080/10426509708043544

The three steps synthesis of new 2-hydrazonophenylthioacetamides having a N-monosubstitued thioamide group is described. The selective acylation of the thioamide nitrogen atom involves an intramolecular cyclisation affording 3,6-dihydro-2H-1,3,4-thiadiazi

Full text of DOI:10.1080/10426509708043544

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Phosphorus, Sulfur, and Silicon and the
Related Elements
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NEW 2-
HYDRAZONOPHENYLTHIOACETAMIDES
INTERMEDIATES IN THE SYNTHESIS OF
6-ACYLAMINO-3,6- DIHYDRO-2H-1,3,4-
THIADIAZINES
M. J. Gil a , A. Reliquet a & J. C. Meslin a
a Laboratoire de Synthése Organique, U. A. C.N.R.S. 475 , 2, rue de la
Houssiniére, 44072, Nantes Cedex, France
Published online: 04 Oct 2006.
To cite this article: M. J. Gil , A. Reliquet & J. C. Meslin (1997) NEW 2-
HYDRAZONOPHENYLTHIOACETAMIDES INTERMEDIATES IN THE SYNTHESIS OF 6-ACYLAMINO-3,6-
DIHYDRO-2H-1,3,4-THIADIAZINES, Phosphorus, Sulfur, and Silicon and the Related Elements, 126:1, 39-52,
DOI: 10.1080/10426509708043544
To link to this article: http://dx.doi.org/10.1080/10426509708043544
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