Publications

Koukal, P.; Ulč, J.; Nečas, D.; Kotora, M. Enantioselective Allylation of β-Haloacrylaldehydes: Formal Total Syntheses of Pteroenone and Antillatoxin. European Journal of Organic Chemistry 2016, 2016 (12), 2110-2114 DOI: 10.1002/ejoc.201600286.

Císařová, I.; Docekal, V.; Petrželová, S.; Vesely, J. Enantioselective Cyclopropanation of 4-Nitroisoxazole Derivatives. Advanced Synthesis and Catalysis 2020, 362 (13), 2597-2603 DOI: 10.1002/adsc.202000231.

Kadlcikova, A.; Vlašaná, K.; Kotora, M. Enantioselective epoxide ring opening catalyzed by bis(tetrahydroisoquinoline) N,N′-dioxides. Collection of Czechoslovak Chemical Communications 2011, 76 (5), 415-422 DOI: 10.1135/cccc2011024.

Vesely, J.; Rios, R. Enantioselective methodologies using N-carbamoyl-imines. Chem. Soc. Rev. 2014, 43 (2), 611-630 DOI: 10.1039/C3CS60321K.

Šimek, M.; Remeš, M.; Vesely, J.; Rios, R. Enantioselective Organocatalytic Amination of Pyrazolones. Asian Journal of Organic Chemistry 2013, 2 (1), 64-68 DOI: 10.1002/ajoc.201200168.

Císařová, I.; Géant, P. Yves; Kamlar, M.; Remeš, M.; Šotolová, M.; Štícha, M.; Veselý, J. Enantioselective Organocatalytic Synthesis of 1,2,3-Trisubstituted Cyclopentanes. European Journal of Organic Chemistry 2021, 2021 (36), 5080-5089.

Géant, P. - Y.; Urban, M.; Remeš, M.; Císařová, I.; Vesely, J. Enantioselective Organocatalytic Synthesis of Sulfur-Containing Spirocyclic Compounds: Organocatalytic Synthesis of Sulfur-Containing Spiro Compounds. European Journal of Organic Chemistry 2013, 2013 (35), 7979-7988 DOI: 10.1002/ejoc.201300931.

Císařová, I.; Kamlar, M.; Nigríni, M.; Reiberger, R.; Veselý, J. Enantioselective PCCP Brønsted acid-catalyzed aminalization of aldehydes. Beilstein Journal of Organic Chemistry 2021, 17 (September), 2433-2440.

Mikušek, J.; Jansa, P.; Jagtap, P. R.; Vasicek, T.; Císařová, I.; Matoušová, E. Enantioselective Synthesis of All-Carbon Quaternary Centers Structurally Related to Amaryllidaceae Alkaloids. Chemistry-a European Journal 2018, 24 (40), 10069-10072 DOI: 10.1002/chem.201802493.

Betík, R.; Kotora, M. Enantioselective Synthesis of (-)-Methoxyestrone. European Journal of Organic Chemistry 2011, 2011 (18), 3279-3282 DOI: 10.1002/ejoc.201100317.

Matoušová, E.; Koukal, P.; Formánek, B.; Kotora, M. Enantioselective Synthesis of the Unsaturated Fragment of Callyspongiolide. Organic Letters 2016, 18 (21), 5656-5659 DOI: 10.1021/acs.orglett.6b02897.

Hanzlová, E.; Váňa, J.; Shaffer, C. J.; Roithová, J.; Martinů, T. Evidence for the Cyclic CN ₂ Carbene in the Gas Phase. Organic Letters 2014, 16 (20), 5482-5485 DOI: 10.1021/ol5027602.

Kurka, O.; Roithová, J.; Bednář, P. Examination of small molecule losses in 5-methylpyranopelargonidin MS/MS CID spectra by DFT calculations: MS/MS and DFT of 5-methylpyranopelargonidin. Journal of Mass Spectrometry 2014, 49 (12), 1314-1321 DOI: 10.1002/jms.3466.

Bojdys, M. J.; Severin, N.; Rabe, J. P.; Cooper, A. I.; Thomas, A.; Antonietti, M. 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.

Srnec, M.; Navrátil, R.; Andris, E.; Jašík, J.; Roithová, J. Experimentally Calibrated Analysis of the Electronic Structure of CuO+: Implications for Reactivity. Angewandte Chemie-International Edition 2018, 57 (52), 17053-17057 DOI: 10.1002/anie.201811362.

Kamlar, M.; Sunden, H.; Zacharias, S. C. Exploring Supramolecular Gels in Flow-Type Chemistry-Design and Preparation of Stationary Phases. Industrial and Engineering Chemistry Research 2021, 60 (28), 10056-10063.

Kochergin, Y. S.; Schwarz, D.; Acharjya, A.; Ichangi, A.; Kulkarni, R.; Eliasova, P.; Vacek, J.; Schmidt, J.; Thomas, A.; Bojdys, M. J. Exploring the "Goldilocks Zone" of Semiconducting Polymer Photocatalysts by Donor-Acceptor Interactions. Angewandte Chemie-International Edition 2018, 57 (43), 14188-14192 DOI: 10.1002/anie.201809702.

Novák, P.; Pour, M.; Špulák, M.; Votruba, I.; Kotora, M. Extension of the Library of Biologically Active γ-Alkylidene Butenolides. Synthesis 2008, 2008 (21), 3465-3472 DOI: 10.1055/s-0028-1083181.

Nečas, D.; Drabina, P.; Sedlák, M.; Kotora, M. Fe-Catalyzed reactions of 2-chloro-1,7-dienes and allylmalonates. Tetrahedron Letters 2007, 48 (26), 4539-4541 DOI: 10.1016/j.tetlet.2007.04.143.

Forster, R. J.; Hocek, M.; Magriñá, I.; Ortiz, M.; O'Sullivan, C. Kathleen; Simonova, A. Ferrocene-Containing DNA Monolayers: Influence of Electrostatics on the Electron Transfer Dynamics. Langmuir : the ACS journal of surfaces and colloids 2021, 37 (11), 3359-3369.

Bultel-Ponce, V.; Durand, T.; Galano, J. - M.; Guy, A.; Jahn, U.; Oger, C.; Pavlíčková, T.; Reversat, G.; Rocher, A.; Vigor, C. First Total Syntheses of Novel Non-Enzymatic Polyunsaturated Fatty Acid Metabolites and Their Identification in Edible Oils. Chemistry - A European Journal 2020, 26 (44), 10090-10098 DOI: 10.1002/chem.202002138.

Hartman, T.; Herzig, V.; Buděšínský, M.; Jindřich, J.; Cibulka, R.; Kraus, T. Flavin–cyclodextrin conjugates: effect of the structure on the catalytic activity in enantioselective sulfoxidations. Tetrahedron: Asymmetry 2012, 23 (22–23), 1571-1583 DOI: 10.1016/j.tetasy.2012.10.017.

Kielkowski, P.; Cahová, H.; Pohl, R.; Hocek, M. Flexible double-headed cytosine-linked 2′-deoxycytidine nucleotides. Synthesis, polymerase incorporation to DNA and interaction with DNA methyltransferases. Bioorganic & Medicinal Chemistry 2016, 24 (6), 1268-1276 DOI: 10.1016/j.bmc.2016.01.057.

Ménová, P.; Dziuba, D.; Güixens-Gallardo, P.; Jurkiewicz, P.; Hof, M.; Hocek, M. Fluorescence Quenching in Oligonucleotides Containing 7-Substituted 7-Deazaguanine Bases Prepared by the Nicking Enzyme Amplification Reaction. Bioconjugate Chemistry 2015, 26 (2), 361-366 DOI: 10.1021/acs.bioconjchem.5b00006.

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.