Crossref Cited-by Linking logo

Collect. Czech. Chem. Commun. 2007, 72, 347-362
https://doi.org/10.1135/cccc20070347

Heterocyclization of (Acridin-9-yl)thiosemicarbazides with Dimethyl Acetylenedicarboxylate

Jana Tomaščikováa, Ján Imricha,*, Ivan Danihela, Stanislav Böhmb and Pavol Kristiana

a Institute of Chemistry, Faculty of Science, P. J. Šafárik University, SK-041 67 Košice, Slovak Republic
b Department of Organic Chemistry, Institute of Chemical Technology, Prague, CZ-166 28 Prague 6, Czech Republic

Crossref Cited-by Linking

  • Hassan Alaa A., Makhlouf Maysa M.: Thiazolidine‐4‐ones from Thiocarbohydrazides. Journal of Heterocyclic Chem 2018, 55, 2480. <https://doi.org/10.1002/jhet.3315>
  • M. Riyadh Sayed, M. Gomha Sobhi, M. Abbas Ikhlass, A. Bauomi Mohammed: Synthetic Utility of Ethylidenethiosemicarbazide: Synthesis and Anticancer Activity of 1,3-Thiazines and Thiazoles with Imidazole Moiety. HETEROCYCLES 2013, 87, 341. <https://doi.org/10.3987/COM-12-12625>
  • Paulíková Helena, Vantová Zuzana, Hunáková Ľuba, Čižeková Lýdia, Čarná Mária, Kožurková Mária, Sabolová Danica, Kristian Pavol, Hamuľaková Slávka, Imrich Ján: DNA binding acridine–thiazolidinone agents affecting intracellular glutathione. Bioorganic & Medicinal Chemistry 2012, 20, 7139. <https://doi.org/10.1016/j.bmc.2012.09.068>
  • Antosova Andrea, Chelli Beatrice, Bystrenova Eva, Siposova Katarina, Valle Francesco, Imrich Jan, Vilkova Maria, Kristian Pavol, Biscarini Fabio, Gazova Zuzana: Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme. Biochimica et Biophysica Acta (BBA) - General Subjects 2011, 1810, 465. <https://doi.org/10.1016/j.bbagen.2011.01.007>
  • Potočňák Ivan, Imrich Ján, Danihel Ivan, Kožíšek Jozef, Klika Karel Douglas: 4-(9,10-Dihydroacridin-9-ylidene)thiosemicarbazide and its five-membered thiazole and six-membered thiazine derivatives. Acta Crystallogr C Cryst Struct Commun 2010, 66, o87. <https://doi.org/10.1107/S0108270110001277>
  • 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>
  • Fröhlichová Zdenka, Imrich Ján, Danihel Ivan, Kristian Pavol, Böhm Stanislav, Sabolová Danica, Kožurková Mária, Hritzová Ol’ga, Horváth Branislav, Bušová Tatiana: Spectroscopic, structural and theoretical studies of novel, potentially cytotoxic 4-acridonecarboxamide imines. Spectochim Acta A 2009, 73, 238. <https://doi.org/10.1016/j.saa.2009.02.016>
  • B��hm Stanislav, Toma����ikov�� Jana, Imrich J��n, 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, ��-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>
  • Gazova Zuzana, Bellova Andrea, Daxnerova Zuzana, Imrich Jan, Kristian Pavol, Tomascikova Jana, Bagelova Jaroslava, Fedunova Diana, Antalik Marian: Acridine derivatives inhibit lysozyme aggregation. Eur Biophys J 2008, 37, 1261. <https://doi.org/10.1007/s00249-008-0313-0>
  • Tomaščiková Jana, Imrich Ján, Danihel Ivan, Böhm Stanislav, Kristian Pavol, Pisarčíková Jana, Sabol Marián, Klika Karel D.: Regioselectivity and Tautomerism of Novel Five-Membered Ring Nitrogen Heterocycles Formed via Cyclocondensation of Acylthiosemicarbazides. Molecules 2008, 13, 501. <https://doi.org/10.3390/molecules13030501>
  • Tomascikova Jana, Imrich Jan, Danihel Ivan, Boehm Stanislav, Kristian Pavol: Heterocyclization of (Acridin‐9‐yl)thiosemicarbazides with Dimethyl Acetylenedicarboxylate. ChemInform 2007, 38. <https://doi.org/10.1002/chin.200736133>