Synthesis of 4-thioacetyl-1,2,3-thiadiazoles. Reversible rearrangement of N-substituted 5-methyl-1,2,3-thiadiazole-4-carbothioamides / Prokhorova P.E., Kalinina T.A., Glukhareva T.V., Morzherin Y.Y. // Russian Journal of Organic Chemistry. - 2012. - V. 48, l. 10. - P. 1333-1336.

ISSN:
10704280
Type:
Article
Abstract:
The equilibrium in the reversible rearrangement of 5-methyl-1,2,3- thiadiazole-4-carbothioamides into 5-amino-4-thioacetyl-1,2,3-thiadiazoles is displaced toward the former, and polar solvents favor increased fraction of the thioketone. © Pleiades Publishing, Ltd., 2012.
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DOI:
10.1134/S1070428012100132
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Affiliations Yeltsin Ural Federal University, ul. Mira 19, Yekaterinburg, 620002, Russian Federation
References Bakulev, V.A., Dehaen, W., (2004) The Chemistry of 1,2,3-Thiadiazoles, , Hoboken, NJ: Wiley; Regitz, M., Liedhegener, A., (1967) Justus Liebigs Ann. Chem, 710, p. 118; Morzherin, Yu.Yu., Bakulev, V.A., Dankova, E.F., Mokrushin, V.S., (1994) Khim. Geterotsikl. Soedin, p. 548; Reichardt, C., (1988) Solvents and Solvent Effects in Organic Chemistry, , Weinheim: VCH, 2nd ed; Frisch, M.J., Trucks, G.W., Schlegel, H.B., Scuseria, G.E., Robb, M.A., Cheeseman, J.R., Montgomery Jr., J.A., Pople, J.A., (2004) Gaussian 03, Revision A.1, , Wallingford CT: Gaussian
Correspondence Address Prokhorova, P.E.; Yeltsin Ural Federal University, ul. Mira 19, Yekaterinburg, 620002, Russian Federation
CODEN RJOCE
Language of Original Document English
Abbreviated Source Title Russ. J. Org. Chem.
Source Scopus