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Collect. Czech. Chem. Commun. 2007, 72, 1435-1445
https://doi.org/10.1135/cccc20071435

Theoretical Confirmation of the Reaction Mechanism Leading to Regioselective Formation of Thiazolidin-4-one from Bromoacetic Acid Derivatives

Ladislav Janoveca, Stanislav Böhmb, Ivan Danihela, Ján Imricha,*, Pavol Kristiana and Karel D. Klikac

a Institute of Chemistry, Faculty of Science, P. J. Šafárik University, SK-04167 Košice, Slovak Republic
b Department of Organic Chemistry, Institute of Chemical Technology, Prague, CZ-16628 Prague 6, Czech Republic
c Department of Chemistry, University of Turku, FIN-20014 Turku, Finland

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  • Imrich Ján, Tomaščiková Jana, Danihel Ivan, Kristian Pavol, Böhm Stanislav, D. Klika Karel: Selective Formation of 5- or 6-Membered Rings, 1,3-Thiazolidin-4-one vs. 1,3-Thiazin-4-one, from Acridine Thiosemicarbazides by the Use of Ethyne Acid Esters. HETEROCYLES 2010, 80, 489. <https://doi.org/10.3987/COM-09-S(S)56>
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  • Böhm Stanislav, Tomaščiková Jana, Imrich Ján, Danihel Ivan, Kristian Pavol, Koch Andreas, Kleinpeter Erich, Klika Karel D.: Computational study to assign structure, tautomerism, E/Z and s-cis/s-trans isomerism, π-delocalization, partial aromaticity, and the ring size of 1,3-thiazolidin-4-ones and 1,3-thiazin-4-ones formed from thiosemicarbazides. Journal of Molecular Structure: THEOCHEM 2009, 916, 105. <https://doi.org/10.1016/j.theochem.2009.09.019>