Publications

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.

Čihák, M.; Hurný, D.; Malečková, A.; Štuka, Č.; Tonar, Z.; Vejražka, M. "Desatero" akademického pedagoga. https://karlovkaonline.cz/wp-content/uploads/2021/04/UK_fond-desatero_www.pdf, 2021.

Herrmann, P.; Buděšínský, M.; Kotora, M. Zirconocene-mediated Preparation of Precursors for Estratriene Synthesis. Chemistry Letters 2007, 36 (10), 1268-1269 DOI: 10.1246/cl.2007.1268.

Danhel, A.; Raindlová, V.; Havran, L.; Barek, J.; Hocek, M.; Fojta, M. Voltammetric Study of dsDNA Modified by Multi-redox Label Based on N-methyl-4-hydrazino-7-nitrobenzofurazan. Electrochimica Acta 2014, 129, 348-357 DOI: 10.1016/j.electacta.2014.02.137.

Danhel, A.; Raindlová, V.; Havran, L.; Barek, J.; Hocek, M.; Fojta, M. Voltammetric Study of dsDNA Modified by Multi-redox Label Based on N-methyl-4-hydrazino-7-nitrobenzofurazan. Electrochimica Acta 2014, 129, 348-357 DOI: 10.1016/j.electacta.2014.02.137.

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.

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.

Dadová, J.; Orság, P.; Pohl, R.; Brázdová, M.; Fojta, M.; Hocek, M. Vinylsulfonamide and Acrylamide Modification of DNA for Cross-linking with Proteins. Angewandte Chemie International Edition 2013, 52 (40), 10515-10518 DOI: 10.1002/anie.201303577.

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.

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.

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.

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.

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.

Havlikova, M.; Bosakova, Z.; Benkovics, G.; Jindřich, J.; Popr, M.; Coufal, P. Use of 6-O-mono-substituted derivatives of β-cyclodextrin-bearing substituent with two permanent positive charges in capillary electrophoresis. Chemical Papers 2016, 70 (9), 1144–1154 DOI: 10.1515/chempap-2016-0053.

Albiñana, C. Berenguer; Brynda, J.; Fanfrlík, J.; Flieger, M.; Hodek, J.; Karlukova, E.; Konvalinka, J.; Kožíšek, M.; Machara, A.; Majer, P.; et al. Unraveling the anti-influenza effect of flavonoids: Experimental validation of luteolin and its congeners as potent influenza endonuclease inhibitors. European Journal of Medicinal Chemistry 2020, 208 (December), nestránkováno DOI: 10.1016/j.ejmech.2020.112754.

Werner, L.; Wernerova, M.; Machara, A.; Endoma-Arias, M. Ann; Duchek, J.; Adams, D. R.; D. Cox, P.; Hudlicky, T. Unexpected N -Demethylation of Oxymorphone and Oxycodone N -Oxides Mediated by the Burgess Reagent: Direct Synthesis of Naltrexone, Naloxone, and Other Antagonists from Oxymorphone. Advanced Synthesis & Catalysis 2012, 354 (14-15), 2706-2712 DOI: 10.1002/adsc.201200676.

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.

Kotora, M.; Hessler, F.; Eignerová, B. Transition-Metal-Mediated or -Catalyzed Syntheses of Steroids and Steroid-Like Compounds. European Journal of Organic Chemistry 2012, 2012 (1), 29-42 DOI: 10.1002/ejoc.201100921.

Hocek, M.; Ondruš, M.; Sýkorová, V. Traceless enzymatic synthesis of monodispersed hypermodified oligodeoxyribonucleotide polymers from RNA templates. Chemical Communications 2022, 58 (80), 11248-11251.

Kolská, K.; Ghavre, M.; Pour, M.; Hybelbauerová, S.; Kotora, M. Total Synthesis of Coibacin D by Using Enantioselective Allylation and Metathesis Reactions. Asian Journal of Organic Chemistry 2016, 5 (5), 646-651 DOI: 10.1002/ajoc.201600022.

Dian, J.; Holec, T.; Jelinek, I.; Jindrich, J.; Valenta, J.; Pelant, I. Time evolution of photoluminescence response from porous silicon in hydrocarbon gas sensing. Physica Status Solidi A-Applied Research 2000, 182 (1), 485-488 DOI: 10.1002/1521-396X(200011)182:1<485::AID-PSSA485>3.0.CO;2-8.

Gallardo, P. Güixens; Hocek, M.; Hof, M.; Humpolickova, J.; Jurkiewicz, P.; Kraus, T.; Miclea, S. Paul; Pohl, R. Thiophene-linked tetramethylbodipy-labeled nucleotide for viscosity-sensitive oligonucleotide probes of hybridization and protein-DNA interactions. Organic and Biomolecular Chemistry 2020, 18 (5), 912-919 DOI: 10.1039/c9ob02634g.

Gallardo, P. Güixens; Hocek, M.; Hof, M.; Humpolickova, J.; Jurkiewicz, P.; Kraus, T.; Miclea, S. Paul; Pohl, R. Thiophene-linked tetramethylbodipy-labeled nucleotide for viscosity-sensitive oligonucleotide probes of hybridization and protein-DNA interactions. Organic and Biomolecular Chemistry 2020, 18 (5), 912-919 DOI: 10.1039/c9ob02634g.

Gallardo, P. Güixens; Hocek, M.; Hof, M.; Humpolickova, J.; Jurkiewicz, P.; Kraus, T.; Miclea, S. Paul; Pohl, R. Thiophene-linked tetramethylbodipy-labeled nucleotide for viscosity-sensitive oligonucleotide probes of hybridization and protein-DNA interactions. Organic and Biomolecular Chemistry 2020, 18 (5), 912-919 DOI: 10.1039/c9ob02634g.