Drug-like Inhibitors of DC-SIGN Based on a Quinolone Scaffold von Zhang, Hengxi, Daněk, Ondřej, Makarov, Dmytro, Rádl, Stanislav, Kim, Dongyoon, Ledvinka, Jiří, Vychodilová, Kristýna, Hlaváč, Jan, Lefèbre, Jonathan, Denis, Maxime, Rademacher, Christoph, Ménová, Petra

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A Scalable Synthesis of Roxadustat (FG-4592) von Píša, Ondřej, Rádl, Stanislav, Čerňa, Igor, Šembera, Filip

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Synthesis of Fingolimod Employing Regioselective Aziridine Ring-Opening Reaction as a Key Step von Doubský, Jan, Rádl, Stanislav, Cinibulk, Josef, Klvaňa, Robert

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Identification of an Unexpected Impurity in a New Improved Synthesis of Lesinurad von Halama, Aleš, Stach, Jan, Rádl, Stanislav, Benediktová, Kristýna

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Synthesis of 4-Quinolones: N,O-Bis­(trimethylsilyl)acetamide-Mediated Cyclization with Cleavage of Aromatic C-O Bond von Pisa, Ondrej, Radl, Stanislav

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Will the Drugs of the Future Be Small Molecules or Biological Drugs? von Rádl, Stanislav, Dammer, Ondřej, Ridvan, Luděk

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Improved Process for Azilsartan Medoxomil: A New Angiotensin Receptor Blocker von Rádl, Stanislav, Černý, Josef, Stach, Jan, Gablíková, Zuzana

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Identification, characterization, synthesis and HPLC quantification of new process-related impurities and degradation products in retigabine von Douša, Michal, Srbek, Jan, Rádl, Stanislav, Černý, Josef, Klecán, Ondřej, Havlíček, Jaroslav, Tkadlecová, Marcela, Pekárek, Tomáš, Gibala, Petr, Nováková, Lucie

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An Improved Synthesis of Elvitegravir von Rádl, Stanislav, Stach, Jan, Píša, Ondřej, Cinibulk, Josef, Havlíček, Jaroslav, Zajícová, Markéta, Pekárek, Tomáš

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Synthesis of 2-(4-Isopropylthiazol-2-yl)-7-methoxy-8-methylquinolin-4-ol; A Quinoline Building Block for Simeprevir Synthesis von Rádl, Stanislav, Rezková, Hana, Obadalová, Iva, Srbek, Jan, Břicháč, Jiří, Pekárek, Tomáš

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Synthesis of Azilsartan and Its Selected Potential Impurities von Rádl, Stanislav, Černý, Josef, Stach, Jan, Holec, Jan, Píša, Ondřej, Gablíková, Zuzana

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Identification, preparation and UHPLC determination of process-related impurity in zolmitriptan von Douša, Michal, Gibala, Petr, Rádl, Stanislav, Klecán, Ondřej, Mandelová, Zuzana, Břicháč, Jiří, Pekárek, Tomáš

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A synthesis of licofelone using Fenton’s reagent von Rádl, Stanislav, Černý, Josef, Klecán, Ondřej, Stach, Jan, Plaček, Lukáš, Mandelová, Zuzana

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Synthesis of some impurities and/or degradation products of zaleplon von Rádl, Stanislav, Blahovcová, Michaela, Plaček, Lukáš, Pekárek, Tomáš, Havlíček, Jaroslav

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Synthetic studies connected with the preparation of h+/k+-ATPase inhibitors rabeprazole and lansoprazole von Rédl, Stanislav, Klecén, Ondřej, Havlíček, Jaroslav

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AN IMPROVED PRODUCTION METHOD AND NEW INTERMEDIATES OF SYNTHESIS OF ELVITEGRAVIR von RADL, STANISLAV

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AN IMPROVED PRODUCTION METHOD AND NEW INTERMEDIATES OF SYNTHESIS OF ELVITEGRAVIR von STANISLAV RADL

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AN IMPROVED PRODUCTION METHOD AND NEW INTERMEDIATES OF SYNTHESIS OF ELVITEGRAVIR von RADL, Stanislav

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A NEW PRODUCTION METHOD AND NEW INTERMEDIATES OF SYNTHESIS OF ELVITEGRAVIR von RADL, Stanislav

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A METHOD OF MANUFACTURING 2-ETHOXY-1-(2'-((HYDROXYAMINO)IMINOMETHYL)BIPHENYL-4-YL) METHYL)-1H-BENZO(D)IMIDAZOLE-7-CARBOXYLIC ACID AND ITS ESTERS von RADL, Stanislav

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