Publications
Haloalkenyl Imidoyl Halides as Multifacial Substrates in the Stereoselective Synthesis of N-Alkenyl Compounds. Advanced Synthesis and Catalysis 2021, 363 (13), 3258-3266.
En route to local glioblastoma treatment with temozolomide doped hyaluronan fibres: formulation and in vitro cell studies. RSC Medicinal Chemistry 2023, 14 (9), 1662-1666.
Direct Comparison of Analogous Amphiphilic Gradient and Block Polyoxazolines. Macromolecules 2021, 54 (17), 8182-8194.
Supramolecular structures based on regioisomers of cinnamyl-α-cyclodextrins – new media for capillary separation techniques. Beilstein Journal of Organic Chemistry 2016, 12, 97-109 DOI: 10.3762/bjoc.12.11.
Novel beta-cyclodextrin-eosin conjugates. Beilstein Journal of Organic Chemistry 2017, 13, 543-551 DOI: 10.3762/bjoc.13.52.
The 'Visualized' macrocycles: Chemistry and application of fluorophore tagged cyclodextrins. International Journal of Pharmaceutics 2017, 531 (2), 689-700 DOI: 10.1016/j.ijpharm.2017.04.035.
1,2,4-Thiadiazole acyclic nucleoside phosphonates as inhibitors of cysteine dependent enzymes cathepsin K and GSK-3β. Bioorganic & Medicinal Chemistry 2021, 32 (February), nestránkováno.
Synthesis of an (±)-Estrone Precursor: The Scope of Zr- and Co-Mediated Cycloannulations. European Journal of Organic Chemistry 2010, 2010 (4), 646-655 DOI: 10.1002/ejoc.200900937.
Enantioselective Synthesis of (-)-Methoxyestrone. European Journal of Organic Chemistry 2011, 2011 (18), 3279-3282 DOI: 10.1002/ejoc.201100317.
Catalytic Cyclotrimerization Pathway for Synthesis of Selaginpulvilins C and D: Scope and Limitations. Organic Letters 2021, 23 (12), 4511-4515.
Catalytic asymmetric addition to cyclic N-acyl-iminium: Access to sulfone-bearing contiguous quaternary stereocenters. Chemical Communications 2022, 58 (71), 9942-9945.
Catalytic approach to unsymmetrical [7]-helical indenofluorenes: Cyclotrimerization vs. dehydro-Diels-Alder reaction pathways. Catalysis Today 2022, 390-391 (May), 48-56.
Complete Sets of Monosubstituted γ-Cyclodextrins as Precursors for Further Synthesis. The Journal of Organic Chemistry 2013, 78 (2), 697-701 DOI: 10.1021/jo301656p.
Mo-Catalyzed Cross-Metathesis Reaction of Propynylferrocene. European Journal of Inorganic Chemistry 2008, 2008 (25), 3911-3920 DOI: 10.1002/ejic.200800128.
Sonogashira reactions of α- and β-1-ethynyl-2-deoxyribosides: synthesis of acetylene-extended C-nucleosides. Tetrahedron 2010, 66 (2), 530-536 DOI: 10.1016/j.tet.2009.11.030.
2D or not 2D-Layered Functional (C, N) Materials “Beyond Silicon and Graphene”. Macromolecular Chemistry and Physics 2016, 217 (2), 232-241 DOI: 10.1002/macp.201500312.
Ionothermal Synthesis of Crystalline, Condensed, Graphitic Carbon Nitride. Chemistry - A European Journal 2008, 14 (27), 8177-8182 DOI: 10.1002/chem.200800190.
Rational Extension of the Family of Layered, Covalent, Triazine-Based Frameworks with Regular Porosity. Advanced Materials 2010, 22 (19), 2202-2205 DOI: 10.1002/adma.200903436.
Ionothermal Route to Layered Two-Dimensional Polymer-Frameworks Based on Heptazine Linkers. Macromolecules 2010, 43 (16), 6639-6645 DOI: 10.1021/ma101008c.
Supramolecular Engineering of Intrinsic and Extrinsic Porosity in Covalent Organic Cages. Journal of the American Chemical Society 2011, 133 (41), 16566-16571 DOI: 10.1021/ja2056374.
Porous organic cage crystals: characterising the porous crystal surface. Chemical Communications 2012, 48 (98), 11948 DOI: 10.1039/c2cc36602a.
Exfoliation of Crystalline 2D Carbon Nitride: Thin Sheets, Scrolls and Bundles via Mechanical and Chemical Routes. Macromolecular Rapid Communications 2013, 34 (10), 850-854 DOI: 10.1002/marc.201300086.
6-Aryl-4-amino-pyrimido[4,5-b]indole 2′-deoxyribonucleoside triphosphates (benzo-fused 7-deaza-dATP analogues): Synthesis, fluorescent properties, enzymatic incorporation into DNA and DNA-protein binding study. Bioorganic & Medicinal Chemistry 2016, 24 (19), 4528-4535 DOI: 10.1016/j.bmc.2016.07.054.
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.
Structure-based design and modular synthesis of novel PI4K class II inhibitors bearing a 4-aminoquinazoline scaffold. Bioorganic and Medicinal Chemistry Letters 2022, 76 (November), nestránkováno.