Publications

Vesely, J.; Ledvina, M.; Jindřich, J.; Šaman, D.; Trnka, T. Improved Synthesis of 1,2-trans-Acetates and 1,2-trans Ethyl 1-Thioglycosides Derived from 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-D-hexopyranosides. Collection of Czechoslovak Chemical Communications 2003, 68 (7), 1264-1274 DOI: 10.1135/cccc20031264.

Zhang, K.; Meazza, M.; Docekal, V.; Light, M. E.; Vesely, J.; Rios, R. Highly Diastereo- and Enantioselective Synthesis of alpha-Spiro-delta-lactams by an Organocascade Reaction. European Journal of Organic Chemistry 2017, No. 13, 1749-1756 DOI: 10.1002/ejoc.201700193.

Schwarz, D.; Acharja, A.; Ichangi, A.; Lyu, P.; Opanasenko, M. V.; Gossler, F. R.; Konig, T. A. F.; Cejka, J.; Nachtigall, P.; Thomas, A.; et al. Fluorescent Sulphur- and Nitrogen-Containing Porous Polymers with Tuneable Donor-Acceptor Domains for Light-Driven Hydrogen Evolution. Chemistry-a European Journal 2018, 24 (46), 11916-11921 DOI: 10.1002/chem.201802902.

Bělinová, T.; Beneš, H.; Groborz, O.; Heizer, T.; Herynek, V.; Hrubý, M.; Loukotová, L.; Raabová, H.; Švec, P. Direct Comparison of Analogous Amphiphilic Gradient and Block Polyoxazolines. Macromolecules 2021, 54 (17), 8182-8194.

Mateus, M. Alexandre; Lapinskaite, R.; Malatinec, Š.; Rýček, L. 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.

Groborz, O.; Holubová, M.; Hromádková, J.; Hrubý, M.; Lobaz, V.; Loukotová, L.; Pechrová, Z.; Rabyk, M.; Štěpánek, P.; Trhlíková, O. Chemically modified glycogens: How they influence formation of amyloid fibrils?. Soft Matter 2021, 17 (6), 1614-1627.

Groborz, O.; Holubová, M.; Hromádková, J.; Hrubý, M.; Lobaz, V.; Loukotová, L.; Pechrová, Z.; Rabyk, M.; Štěpánek, P.; Trhlíková, O. Chemically modified glycogens: How they influence formation of amyloid fibrils?. Soft Matter 2021, 17 (6), 1614-1627.

Báječný, M.; Beneš, J.; Czernek, J.; Dunlop, D.; Francová, P.; Groborz, O.; Heizer, T.; Hobza, P.; Hrubý, M.; Kolouchová, K.; et al. Chelating Polymers for Hereditary Hemochromatosis Treatment. Macromolecular Bioscience 2020, 20 (12), nestránkováno DOI: 10.1002/mabi.202000254.

Balintová, J.; Simonova, A.; Bialek-Pietras, M.; Olejniczak, A.; Lesnikowski, Z. J.; Hocek, M. Carborane-linked 2 '-deoxyuridine 5 '-O-triphosphate as building block for polymerase synthesis of carborane-modified DNA. Bioorganic & Medicinal Chemistry Letters 2017, 27 (21), 4786-4788 DOI: 10.1016/j.bmcl.2017.09.064.

Fojta, M.; Havran, L.; Hocek, M.; Kodr, D.; Lesnikowski, Z. J.; Ortiz, M.; O'Sullivan, C. Kathleen; Pohl, R.; Saftić, D. Pavlović; Simonova, A.; et al. Carborane- or Metallacarborane-Linked Nucleotides for Redox Labeling. Orthogonal Multipotential Coding of all Four DNA Bases for Electrochemical Analysis and Sequencing. Journal of the American Chemical Society 2021, 143 (18), 7124-7134.

Brynda, J.; Fanfrlík, J.; Hadzima, M.; Hánová, I.; Horn, M.; Houštecká, R.; Lepšík, M.; Majer, P.; Mareš, M.; Mertlíková-Kaiserová, H.; et al. Biomimetic Macrocyclic Inhibitors of Human Cathepsin D: Structure-Activity Relationship and Binding Mode Analysis. Journal of Medicinal Chemistry 2020, 63 (4), 1576-1596 DOI: 10.1021/acs.jmedchem.9b01351.

Bricout, H.; Caronia, E.; Galia, A.; Tichá, I. Chena; Jindřich, J.; Léger, B.; Menuel, S.; Monflier, É.; Noël, S.; Ponchel, A.; et al. Asymmetric hydrogenation of ethyl pyruvate over aqueous dispersed Pt nanoparticles stabilized by a cinchonidine-functionalized β-cyclodextrin. Catalysis Communications 2021, 150 (February), nestránkováno.

Luger, P.; Denner, L.; Cerny, M.; Jindřich, J.; Trnka, T. 16-Crown-5 derivative of 1,6-anhydro-[beta]-D-glucopyranose: structure of [1,6-anhydro-2,4-di-O-(3,6,9-trioxaundecane-1,11-diyl)-[beta]-D-glucopyranose]sodium tetraphenylborate. Acta Crystallographica, Section C: Structural Chemistry 1991, C47, 66-70 DOI: 10.1107/S0108270190007090.

Banwell, M. G.; Buckler, J. N.; Jackson, C. J.; Lan, P.; Ma, X.; Matoušová, E.; Nugent, J. Devising New Syntheses of the Alkaloid Galanthamine, a Potent and Clinically Deployed Inhibitor of Acetylcholine Esterase; Elsevier, 2015; Vol. 11, pp 29-50.