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Collect. Czech. Chem. Commun. 2003, 68, 1243-1263
https://doi.org/10.1135/cccc20031243

Syntheses and Structure Study on 3,3aλ4,4-Trithia-1-azapentalenes and Their 3-Oxa Analogues

Richard Čmelíka, Michal Čajanb, Jaromír Marekc and Pavel Pazderaa,*

a Department of Organic Chemistry, Faculty of Science, Masaryk University, Kotlářská 2, CZ-611 37 Brno, Czech Republic
b National Centre for Biomolecular Research, Faculty of Science, Masaryk University, Kotlářská 2, CZ-611 37 Brno, Czech Republic
c Laboratory of Functional Genomics and Proteomics, Masaryk University, Kotlářská 2, CZ-611 37 Brno, Czech Republic

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  • Rakitin Oleg: Synthesis and Reactivity of 3H-1,2-dithiole-3-thiones. Molecules 2021, 26, 3595. <https://doi.org/10.3390/molecules26123595>
  • Brown Dennis A., Betharia Swati, Yen Jui-Hung, Kuo Ping-Chang, Mistry Hitesh: Further structure–activity relationships study of substituted dithiolethiones as glutathione-inducing neuroprotective agents. Chemistry Central Journal 2016, 10. <https://doi.org/10.1186/s13065-016-0210-z>
  • Rašović Aleksandar, Koch Andreas, Kleinpeter Erich, Marković Rade: Studies of the regioselective ring-opening–closing mode of functionally different thiazolidine type enaminones: en route to the synthesis of trithiaazapentalene derivatives. Tetrahedron 2013, 69, 10849. <https://doi.org/10.1016/j.tet.2013.10.088>
  • Rašović Aleksandar, Steel Peter J., Kleinpeter Erich, Marković Rade: Regioselective synthesis of 1,3-thiazines by sequential 4-oxothiazolidine to 1,2-dithiole to 1,3-thiazine transformations: role of intramolecular non-bonded S⋯O interactions. Tetrahedron 2007, 63, 1937. <https://doi.org/10.1016/j.tet.2006.12.075>
  • Čmelík Richard, Pazdera Pavel: Transformation of 1,2-Dithiole-3-thiones Into 1,6,6aλ4-Trithiapentalenes via Reaction with Bromoethanones. Collect. Czech. Chem. Commun. 2006, 71, 650. <https://doi.org/10.1135/cccc20060650>
  • Cmelik Richard, Cajan Michal, Marek Jaromir, Pazdera Pavel: Syntheses and Structure Study on 3,3aλ4,4‐Trithia‐1‐aza‐pentalenes and Their 3‐Oxa Analogues. ChemInform 2003, 34. <https://doi.org/10.1002/chin.200347107>