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Tichý, M.; Pohl, R.; Tloušt’ová, E.; Weber, J.; Bahador, G.; Lee, Y. - J.; Hocek, M. Synthesis and biological activity of benzo-fused 7-deazaadenosine analogues. 5- and 6-substituted 4-amino- or 4-alkylpyrimido[4,5-b]indole ribonucleosides. Bioorganic & Medicinal Chemistry 2013, 21 (17), 5362-5372 DOI: 10.1016/j.bmc.2013.06.011.
Tichotová, L.; Matoušová, E.; Špulák, M.; Kuneš, J.; Votruba, I.; Buchta, V.; Pour, M. Synthesis and biological activity of desmethoxy analogues of coruscanone A. Bioorganic & Medicinal Chemistry Letters 2011, 21 (20), 6062-6066 DOI: 10.1016/j.bmcl.2011.08.059.
Nauš, P.; Caletková, O.; Perlíková, P.; Slavětínská, L. Poštová; Tloušťová, E.; Hodek, J.; Weber, J.; Džubák, P.; Hajdúch, M.; Hocek, M. Synthesis and biological profiling of 6- or 7-(het)aryl-7-deazapurine 4′-C-methylribonucleosides. Bioorganic & Medicinal Chemistry 2015, 23 (23), 7422-7438 DOI: 10.1016/j.bmc.2015.10.040.
Bartova, K.; Džubák, P.; Fleuti, M. Heidi; Gurska, S.; Hajdúch, M.; Hocek, M.; Pavliš, P.; Slavětínská, L. Poštová; Tichý, M.; Tloušťová, E. Synthesis and Biological Profiling of Pyrazolo-Fused 7-Deazapurine Nucleosides. Journal of Organic Chemistry 2020, 85 (16), 10539-10551 DOI: 10.1021/acs.joc.0c00928.
Bartova, K.; Džubák, P.; Fleuti, M. Heidi; Gurska, S.; Hajdúch, M.; Hocek, M.; Pavliš, P.; Slavětínská, L. Poštová; Tichý, M.; Tloušťová, E. Synthesis and Biological Profiling of Pyrazolo-Fused 7-Deazapurine Nucleosides. Journal of Organic Chemistry 2020, 85 (16), 10539-10551 DOI: 10.1021/acs.joc.0c00928.
Klečka, M.; Slavětínská, L. Poštová; Tloušťová, E.; Džubák, P.; Hajdúch, M.; Hocek, M. Synthesis and cytostatic activity of 7-arylsulfanyl-7-deazapurine bases and ribonucleosides. Med. Chem. Commun. 2015, 6 (4), 576-580 DOI: 10.1039/C4MD00492B.
Perlíková, P.; Eberlin, L.; Ménová, P.; Raindlová, V.; Slavětínská, L.; Tloušťová, E.; Bahador, G.; Lee, Y. - J.; Hocek, M. Synthesis and Cytostatic and Antiviral Activities of 2′-Deoxy-2′,2′-difluororibo- and 2′-Deoxy-2′-fluororibonucleosides Derived from 7-(Het)aryl-7-deazaadenines. ChemMedChem 2013, 8 (5), 832-846 DOI: 10.1002/cmdc.201300047.
Nauš, P.; Caletková, O.; Konečný, P.; Džubák, P.; Bogdanová, K.; Kolář, M.; Vrbková, J.; Slavětínská, L.; Tloušt’ová, E.; Perlíková, P.; et al. Synthesis, Cytostatic, Antimicrobial, and Anti-HCV Activity of 6-Substituted 7-(Het)aryl-7-deazapurine Ribonucleosides. Journal of Medicinal Chemistry 2014, 57 (3), 1097-1110 DOI: 10.1021/jm4018948.
Vesely, J.; Ledvina, M.; Jindrich, J.; Trnka, T.; Saman, D. Synthesis of 2-amino-2-deoxy-beta-D-galactopyranosyl(1 -> 4)-2-amino-2-deoxy-beta-D-galactopyranosides: Using various 2-deoxy-2-phthalimido-D-galactopyranosyl donors and acceptors. Collection of Czechoslovak Chemical Communications 2004, 69 (10), 1914-1938 DOI: 10.1135/cccc20041914.
Tokarenko, A.; Slavětínská, L. Poštová; Klepetářová, B.; Hocek, M. Synthesis of Benzene and Pyridine 2-C-Methyl-C-ribonucleosides and -nucleotides. European Journal of Organic Chemistry 2015, 2015 (36), 7962-7983 DOI: 10.1002/ejoc.201501219.
Bednaříková, T.; Tošner, Z.; Horský, J.; Jindřich, J. Synthesis of C 3 -symmetric tri(alkylamino) guests and their interaction with cyclodextrins. Journal of Inclusion Phenomena and Macrocyclic Chemistry 2015, 81 (1-2), 141-152 DOI: 10.1007/s10847-014-0443-1.
Malnuit, V.; Smolen, S.; Tichý, M.; Slavětínská, L. Poštová; Hocek, M. Synthesis of Cyclic and Acyclic Nucleoside Phosphonates and Sulfonamides Derived from 6-(Thiophen-2-yl)-7-fluoro-7-deazapurine. European Journal of Organic Chemistry 2019, 2019 (31-32), 5409-5423 DOI: 10.1002/ejoc.201900509.
Džubák, P.; Gurska, S.; Hajdúch, M.; Hocek, M.; Pavliš, P.; Pohl, R.; Tichý, M.; Yang, C. Synthesis, Photophysical Properties, and Biological Profiling of Benzothieno-Fused 7-Deazapurine Ribonucleosides. Journal of Organic Chemistry 2020, 85 (12), 8085-8101 DOI: 10.1021/acs.joc.0c00927.
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Schwarz, D.; Kochergin, Y. S.; Acharjya, A.; Ichangi, A.; Opanasenko, M. V.; Cejka, J.; Lappan, U.; Arki, P.; He, J.; Schmidt, J.; et al. Tailored Band Gaps in Sulfur- and Nitrogen-Containing Porous Donor-Acceptor Polymers. Chemistry-a European Journal 2017, 23 (53), 13023-13027 DOI: 10.1002/chem.201703332.
Schwarz, D.; Kochergin, Y. S.; Acharjya, A.; Ichangi, A.; Opanasenko, M. V.; Cejka, J.; Lappan, U.; Arki, P.; He, J.; Schmidt, J.; et al. Tailored Band Gaps in Sulfur- and Nitrogen-Containing Porous Donor-Acceptor Polymers. Chemistry-a European Journal 2017, 23 (53), 13023-13027 DOI: 10.1002/chem.201703332.
Hurný, D.; Malečková, A.; Štuka, Č.; Tonar, Z.; Vejražka, M. Ten evidence-based recommendations for higher education. Mefanet+ 2021: Cooperation on the effective use of technology in medical and healthcare education reflecting on the challenges of today, 2021, 13-13.
Algara-Siller, G.; Severin, N.; Chong, S. Y.; Björkman, T.; Palgrave, R. G.; Laybourn, A.; Antonietti, M.; Khimyak, Y. Z.; Krasheninnikov, A. V.; Rabe, J. P.; et al. Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie 2014, 126 (29), 7580-7585 DOI: 10.1002/ange.201402191.
Algara-Siller, G.; Severin, N.; Chong, S. Y.; Björkman, T.; Palgrave, R. G.; Laybourn, A.; Antonietti, M.; Khimyak, Y. Z.; Krasheninnikov, A. V.; Rabe, J. P.; et al. Triazine-Based Graphitic Carbon Nitride: a Two-Dimensional Semiconductor. Angewandte Chemie International Edition 2014, 53 (29), 7450-7455 DOI: 10.1002/anie.201402191.
Chong, S. Y.; Jones, J. T. A.; Khimyak, Y. Z.; Cooper, A. I.; Thomas, A.; Antonietti, M.; Bojdys, M. J. Tuning of gallery heights in a crystalline 2D carbon nitride network. J. Mater. Chem. A 2013, 1 (4), 1102-1107 DOI: 10.1039/C2TA01068B.
Schwarz, D.; Noda, Y.; Klouda, J.; Schwarzova-Peckova, K.; Tarabek, J.; Rybacek, J.; Janousek, J.; Simon, F.; Opanasenko, M. V.; Cejka, J.; et al. Twinned Growth of Metal-Free, Triazine-Based Photocatalyst Films as Mixed-Dimensional (2D/3D) van der Waals Heterostructures. Advanced Materials 2017, 29 (40), 1703399 DOI: 10.1002/adma.201703399.
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Havranova-Vidlakova, P.; Kroemer, M.; Sykorova, V.; Trefulka, M.; Fojta, M.; Havran, L.; Hocek, M. Vicinal Diol-Tethered Nucleobases as Targets for DNA Redox Labeling with Osmate Complexes. Chembiochem 2019 DOI: 10.1002/cbic.201900388.
Fojta, M.; Havran, L.; Havranova-Vidlakova, P.; Hocek, M.; Krömer, M.; Sykorova, V.; Trefulka, M. Vicinal Diol-Tethered Nucleobases as Targets for DNA Redox Labeling with Osmate Complexes. Chembiochem : a European journal of chemical biology 2020, 21 (1-2), 171-180 DOI: 10.1002/cbic.201900388.
Danhel, A.; Trosanova, Z.; Balintová, J.; Havran, L.; Hocek, M.; Barek, J.; Fojta, M. Voltammetric analysis of 5-(4-Azidophenyl)-2′-deoxycytidine nucleoside and azidophenyl-labelled single- and double-stranded DNAs. Electrochimica Acta 2016, 215, 72-83 DOI: 10.1016/j.electacta.2016.08.096.
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