Publications
Copper-catalyzed reactions: Research in the gas phase: COPPER CATALYSIS. Mass Spectrometry Reviews 2016, 35 (1), 85-110 DOI: 10.1002/mas.21464.
Copper-mediated arylsulfanylations and arylselanylations of pyrimidine or 7-deazapurine nucleosides and nucleotides. Org. Biomol. Chem. 2016, 14 (42), 10018-10022 DOI: 10.1039/C6OB01917J.
Covalent Triazine Frameworks Prepared from 1,3,5-Tricyanobenzene. Chemistry of Materials 2013, 25 (9), 1542-1548 DOI: 10.1021/cm303751n.
Cross-Coupling as a Key Step in the Synthesis and Structure Revision of the Natural Products Selagibenzophenones A and B. Catalysts [online] 2021, 11 (6), nestránkováno.
Cross-Coupling Reaction of Saccharide-Based Alkenyl Boronic Acids with Aryl Halides: The Synthesis of Bergenin. Chemistry - A European Journal 2014, 20 (15), 4414-4419 DOI: 10.1002/chem.201304304.
Cross-Cyclotrimerization with Two Nitriles as a Synthetic Pathway to Unsymmetrically 3,3’-Disubstituted bis(Tetrahydroisoquinolines). Molecules 2009, 14 (8), 2918-2926 DOI: 10.3390/molecules14082918.
Cross-metathesis of allylcarboranes with O-allylcyclodextrins. Beilstein Journal of Organic Chemistry 2010, 6, 1099-1105 DOI: 10.3762/bjoc.6.126.
Cross-metathesis reaction of α- and β-vinyl C -glycosides with alkenes. Beilstein Journal of Organic Chemistry 2015, 11, 1392-1397 DOI: 10.3762/bjoc.11.150.
Cycloaddition Reactions of Deoxyribosylpropynoates. Synthetic Communications 2014, 44 (9), 1232-1239 DOI: 10.1080/00397911.2013.848896.
Cyclodextrin-based Schiff base pro-fragrances: Synthesis and release studies. Beilstein Journal of Organic Chemistry 2022, 18 (September), 1346-1354.
Cyclodextrins and their derivatives - Synthesis and utilization. Chemicke Listy 1997, 91 (11), 956-1032.
. Cyclotrimerization Approach to Symmetric [9]Helical Indenofluorenes: Diverting Cyclization Pathways. Chemistry - A European Journal 2023, 29 (58).
C–H Phosphonation of Pyrrolopyrimidines: Synthesis of Substituted 7- and 9-Deazapurine-8-phosphonate Derivatives. The Journal of Organic Chemistry 2016, 81 (19), 9507-9514 DOI: 10.1021/acs.joc.6b01970.
Decarboxylative Organocatalytic Allylic Amination of Morita-Baylis-Hillman Carbamates. Chemistry-a European Journal 2018, 24 (51), 13441-13445 DOI: 10.1002/chem.201803677.
Design and Synthesis of Novel HIV-1 NNRTIs with Bicyclic Cores and with Improved Physicochemical Properties. Journal of Medicinal Chemistry 2023, 66 (3), 1761-1777.
Design Strategies in Hydrothermal Polymerization of Polyimides. Macromolecular Chemistry and Physics 2016, 217 (3), 485-500 DOI: 10.1002/macp.201500287.
Design, synthesis and evaluation of novel thieno[2,3d]pyrimidine derivatives as potent and specific RIPK2 inhibitors. Bioorganic and Medicinal Chemistry Letters 2024, 97 (1 January 2024).
Design, Synthesis, Biological Evaluation, and Crystallographic Study of Novel Purine Nucleoside Phosphorylase Inhibitors. Journal of Medicinal Chemistry 2023, 66 (10), 6652-6681.
Detection of Indistinct Fe-N Stretching Bands in Iron(V) Nitrides by Photodissociation Spectroscopy. Chemistry-a European Journal 2018, 24 (20), 5078-5081 DOI: 10.1002/chem.201705307.
Determination of cyclodextrin content using periodate oxidation by capillary electrophoresis. Journal of Chromatography A 2000, 891 (1), 201-206 DOI: 10.1016/S0021-9673(00)00628-2.
Determination of cyclodextrins and their derivatives by capillary electrophoresis with indirect UV and conductivity detection. Fresenius Journal of Analytical Chemistry 2001, 369 (7-8), 666-669 DOI: 10.1007/s002160100721.
Determination of sensoric parameters of porous silicon in sensing of organic vapors. Materials Science and Engineering: C 2002, 19 (1-2), 251-254 DOI: 10.1016/S0928-4931(01)00394-0.
Development of a Ratiometric Fluorescent Probe with Two Reactive Sulfoxides for Monitoring the Activity of Methionine Sulfoxide Reductase A. Synthesis-Stuttgart 2018, 50 (4), 772-777 DOI: 10.1055/s-0036-1591888.
Development of a simple high-throughput assay for directed evolution of enantioselective sulfoxide reductases. Chemical Communications 2020, 56 (40), 5386-5388 DOI: 10.1039/d0cc01660h.