Publikace našich autorů

2024

• Niziński S., Varma N.,  Sikorski M.,  Tobrman T., Svobodová E., Cibulka R., Rode M. F., Burdzinski G.:
  Fast singlet excited-state deactivation pathway of flavin with a trimethoxyphenyl derivative.
  Sci Rep  2024, 14, 24375. DOI: 10.1038/s41598-024-75239-x.
  
  
• Weisheitelová I., Cibulka R., Sikorski M., Pavlovska T.:
  A facile three-component route to powerful 5-aryldeazaalloxazine photocatalysts. 
  Beilstein J. Org. Chem. 2024, 20, 1831–1838. DOI: 10.3762/bjoc.20.161.
  

• Venkatraman R. K., Hassan Tolba A., Solling T., Cibulka R., El-Zohry A.:
  Ultrafast Events of Photoexcited Iron(III)chloride for Activation of Benzylic C—H Bonds. 
  J. Phys. Chem. Lett. 2024, 15, 6202−6208, DOI: 10.1021/acs.jpclett.4c011 
  
  
• Weisheitelová I., Varma N., Chudoba J., Burdziński G., Sikorski M., Cibulka R.:
  Catalyst-free aerobic photooxidation of sensitive benzylic alcohols with chemoselectivity controlled by DMSO solvent. 
  Green Chem. 2024, 26, 4880-4887, https://doi.org/10.1039/D4GC00087K
  
  
• Burešová Z., Gobeze H. B., Grygarová M., Pytela O., Klikar M., Obertík R.,  Cibulka R., Islam T., Schanze K. S., Bureš F.:
  Dicyanopyrazine Photoredox Catalysts: Correlation of Efficiency with Photophysics and Electronic Structure. 
  J. Catal. 2024, 430, 115348, DOI: 10.1016/j.jcat.2024.115348
  
  
• Salvadori, K.; Churý, M.; Budka, J.; Harvalík, J.; Matějka, P.; Šimková, L.; Lhoták, P.: 
  Chemoselective Electrochemical Cleavage of Sulfonimides as a Direct Way to Sulfonamides.
  J. Org. Chem. 2024, 89, 1425–1437, https://doi.org/10.1021/acs.joc.3c01932
  
  
  
  

  2023
   

• Zubova, E., Pokluda A., Dvořáková, H., Krupička M., Cibulka R.:
  Exploring the Reactivity of Flavins with Nucleophiles Using a Theoretical and Experimental Approach. 
  ChemPlusChem 2023, Accepted. DOI:10.1002/cplu.202300547.
  
  
• Pavlovska T., Weisheitelová I., Pramthaisong C., Sikorski M., Jahn U., Cibulka R.:
  Primary and Secondary Amines by Flavin‐Photocatalyzed Consecutive Desulfonylation and Dealkylation of Sulfonamides. 
  Adv. Synth. Catal. 2023, 365, 4662-4671. DOI:10.1002/adsc.202300843.
  
  
• Golczak A., Prukała D., Gierszewski M., Cherkas V., Kwiatek D., Kubiak A., Varma N., Pedziński T., Murphree S., Cibulka R., Mrówczińska L., Kolanovski J. L., Sikorski M.:
  Tetramethylalloxazines as efficient singlet oxygen photosensitizers and potential redox‑sensitive agents, Scientific Reports 2023, 13, 13426. DOI: 10.1038/s41598-023-40536-4.
  
  
• Pokluda A., Zubova, E., Chudoba J., Krupička M., Cibulka R.:
  Catalytic Artificial Nitroalkane Oxidases – a Way Towards Organocatalytic Umpolung. 
  Org. Biomol. Chem. 2023, 2768 – 2774. DOI: 10.1039/d3ob00101f.
  
  
• Jurásek, B.; Fagan, P.; Dolenský, B.; Paškanová, N.; Dobšíková, K.; Raich, I.; Jurok, R.; Setnička, V.; Kohout, M.; Čejka, J.; Kuchař, M.:
  A structural spectroscopic study of dissociative anaesthetic methoxphenidine. New J. Chem. 2023, 47, 4543.
  https://doi.org/10.1039/d2nj06126k
  
  
• Dobšíková, K.; Javorská, Ž.; Paškan, M.; Spálovská, D.; Trembuláková, P.; Herciková, J.; Kuchař, M.; Kozmík, V.; Kohout, M.; Setnička, V.:
  Enantioseparation and a comprehensive spectroscopic analysis of novel synthetic cathinones laterally substituted with a trifluoromethyl group. Spectrochim. Acta, Part A, 2023, 291, 122320.
  https://doi.org/10.1016/j.saa.2023.122320
  
  
  

2022

• Cortés F.R., Eigner V., Cuřínová P., Himl M.: 
  Structurally Forced Ion Binding Affinity: Tetraurea-Based Macrocycle as a Receptor for Ion Pairs
  Eur. J. Org. Chem.  2022, e202200, DOI: 10.1002/ejoc.202200422
  
  
• Obertík R., Chudoba J., Šturala J., Tarábek J., Ludvíková L., Slanina T., König B., Cibulka R.:
  Highly Chemoselective Catalytic Photooxidations Using Solvent as a Sacrificial Electron Acceptor
  Chem. Eur. J. 2022, accepted as VIP, https://doi.org/10.1002/chem.202202487
  
  
  
  
• Liška, A.; Řezanková, M.; Klíma, J.; Urban, J.; Budka, J.; Ludvík, J.:
  Electrochemical, EPR, and quantum chemical study of reductive cleavage of cone-Calix[4]arene nosylates – New electrosynthetic approach
  Electrochem. Sci. Adv. 2022, e2100221, DOI: org/10.1002/elsa.202100221
  
  
• Zhang, H.; Daněk, O.; Makarov, D.; Rádl, S.; Kim, D.; Ledvinka, J.; Vychodilová, K.; Hlaváč, J.; Lefèbre, J; Denis, M.; Rademacher, C. and Ménová, P.:
  Drug-like Inhibitors of DC-SIGN Based on a Quinolone Scaffold
  ACS Med. Chem. Lett. 2022, accepted. DOI: 10.1021/acsmedchemlett.2c00067
  
  
• Pavlovska T., Král Lesný D., Svobodová E., Hoskovcová I., Archipowa N., Kutta R. J., Cibulka R.: 
  Tuning Deazaflavins Towards Highly Potent Reducing Photocatalysts Guided by Mechanistic Understanding - Enhancement of the Key Step by the Internal Heavy Atom Effect. Chem. Eur. J. 2022, 2022, 28, e20220076. Hot Paper. DOI: 10.1002/chem.202200768

• Linhart, I.:
  Toxikologie: Interakce škodlivých látek s živými organismy, jejich mechanismy, projevy a důsledky
  VŠCHT Praha 2022 (3. vydání), ISBN 978-80-7592-103-1

• Linhart, I.; Himl, M.; Urban, V.; Mráz, J.:
  Syntheses of methylcarbamoylated amino acids using synthetic equivalents of methyl isocyanate.
  Synth. Commun. 2022, 52, 622-628. DOI: 10.1080/00397911.2022.2042563
  
  
• Paškan, M.; Rimpelová, S.; Svobodová Pavlíčková, V.; Spálovská, D.; Setnička, V.; Kuchař, M.; Kohout, M.:
  4-Isobutylmethcathinone—A novel synthetic cathinone with high in vitro cytotoxicity and strong receptor binding preference of enantiomers. Pharmaceuticals 2022, 15, 1495.
  https://doi.org/10.3390/ph15121495
  
  
• Poryvai, A.; Šmahel, M.; Švecová, M.; Nemati, A.; Shadpour, S.; Ulbrich, P.; Ogolla, T.; Liu, J.; Novotná, V.; Veverka, M.; Vejpravová J.; Hegmann, T.; Kohout, M.:
  Chiral, magnetic, and photosensitive liquid crystalline nanocomposites based on multifunctional nanoparticles and achiral liquid crystals. ACS Nano, 2022, 16, 11833.-11841.
  https://doi.org/10.1021/acsnano.1c10594
  
  
• Hao, L.; Jing, H.; Xiang, Y.; Iljin, A.; Wang, Y.; Li, H.; Li, Q.; Peng, J.; Kohout, M.:
  Transient optically induced grating and underlying transport process in bent-core nematics. J. Appl. Phys. 2022, 132, 065108.
  https://doi.org/10.1063/5.0096106
  
  
• Sysel, P.; Hovorka, Š.; Kohout, M.; Holakovský, R.; Žádný, J.; Čížek, J.; Izák, P.:
  Optically active polyimides with different thermal histories of their preparation. Chirality 2022, 34, 1151-1161.
  https://doi.org/10.1002/chir.23476
  
  
• Asnin, L.; Herciková, J.; Lindner, W.; Klimova, Y.; Ziganshina, D.; Reshetova, E.; Kohout, M.:
  Chiral separation of dipeptides on Cinchona-based zwitterionic chiral stationary phases under buffer-free reversed-phase conditions. Chirality 2022, 34, 1065-1077.
  https://doi.org/10.1002/chir.23471
  
  
• Malinčík, J.; Kohout, M.; Svoboda, J.; Stulov, S.; Pociecha, D.; Böhmová, Z.; Novotná, V. Photochromic spiropyran-based liquid crystals. J. Mol. Liq. 2022, 346, 117842.
  https://doi.org/10.1016/j.molliq.2021.117842
  
  
• Muraveva, V.; Kozmík, V.; Kohout, M.; Manko, A.; Piryazev, A.; Ivanov, D.; Abramchuk, S.; Cigl, M.; Bobrovsky, A.:
  The smectogenicity as a crucial factor of broadening of the selective light reflection peak in cholesteric photopolymerizable mixtures. Liq. Cryst. 2022, 49, 1459-1465.
  https://doi.org/10.1080/02678292.2022.2041745
  
  
• Štefková-Mazochová, K.; Danda, H.; Dehaen, W.; Jurásek, B.; Šíchová, K.; Pinterová-Leca, N.; Mazoch, V.; Krausová, B.H.; Kysilov, B.; Smejkalová, T.; Vyklický, L.; Kohout, M.; Hájková, K.; Svozil, D.; Horsley, R.R.; Kuchař, M.; Páleníček, T.:
  Pharmacokinetic, pharmacodynamic, and behavioural studies of deschloroketamine in Wistar rats. Br. J. Pharmacol. 2022, 179, 65-83.
         https://doi.org/10.1111/bph.15680

2021

• Pokluda A., Anwar Z., Boguschová V., Anusiewicz I., Skurski P., Sikorski M., Cibulka R.:
  Robust photocatalytic method using ethylene-bridged flavinium salts for the aerobic oxidation of unactivated benzylic substrates 
  Adv. Synth. Catal. 2021, 363, 4371-4379. VIP, DOI: 10.1002/adsc.202100024.
  
  
  
  
• Jakubec M., Novák D., Zatloukalová M., Sýkora J., Císařová I., Cibulka R., Favereau L., Crassous J., Bilewicz R., Hrbáč J., Storch J., Žádný J., Vacek J.:
  Flavin-Helicene Amphiphilic Hybrids: Synthesis, Characterization, and Preparation of Surface-Supported Films 
  ChemPlusChem 2021, 86, 982-990. DOI: 10.1002/cplu.202100092
  
  
  
  
• Tolba A. H., Krupička M., Chudoba J., Cibulka R.:
  mide bond formation via aerobic photooxidative coupling of aldehydes with amines catalyzed by a riboflavin derivative 
  Org. Lett. 2021, 23, 6825-6830. DOI: 10.1021/acs.orglett.1c02391

• Tetour, D.; Novotná, M.; Hodačová, J.: 
  Enantioselective Henry Reaction Catalyzed by Copper(II) Complex of Bis(trans-cyclohexane-1,2-diamine)-Based Ligand.
  Catalysts 2021, 11, 41. http:\\dx.doi.org/10.3390/catal11010041
  
  
• Cadart, T.; Nečas, D.; Kaiser, R. P.; Favereau, L.; Císařová, I.; Gyepes, R.; Hodačová, J.; Kalíková, K.; Bednárová, L.; Crassous, J.; Kotora, M.: 
  Rhodium-Catalyzed Enantioselective Synthesis of Highly Fluorescent and CPL Active Dispiroindeno[2,1‐c]fluorenes. 
  Chem. Eur. J. 2021, 27, 11279-11284.https://doi.org/10.1002/chem.202100759
  
  
• Tetour, D.; Paška, T.; Máková, V.; Nikendey Holubová, B.; Karpíšková, J.; Řezanka, M.; Brus, J.; Hodačová, J.: 
  Cinchonine-based organosilica materials as heterogeneous catalysts of enantioselective alkene dihydroxylation. 
  J. Catal. 2021, 404, 493-500. https://doi.org/10.1016/j.jcat.2021.10.015
  
  
• Kortus, D.; Krizova, K.; Dvorakova, H.; Eigner, V.; Lhotak, P.:
  Synthesis of 2,8-dithiacalix[4]arene based on fragment condensation
  Tetrahedron Lett. 2021, 69, 152924 DOI:10.1016/j.tetlet.2021.152924
  
  
• Kortus, D.; Eigner, V.; Lhotak, P.:
  Regio- and stereoselectivity of spirodienone formation in 2,14-dithiacalix[4]arene
  New J. Chem. 2021, 45, 8563-8571 DOI:10.1039/d1nj01257f
  
  
• Kortus, D.; Kundrat, O.; Cejka, J.; Dvorakova, H.; Lhotak, P.:
  Chemistry of 2,14-Dithiacalix[4]arene: Searching for the Missing Fifth Conformer
  J. Org. Chem. 2021 DOI:10.1021/acs.joc.1c01173
  
  
• Curinova, P.; Winkler, M.; Krupkova, A.; Cisarova, I.; Budka, J.; Wun, C.N.; Blechta, V.; Maly, M.; Stastna-Cervenkova, L.; Sykora, J.; Strasak, T.:
  Transport of Anions across the Dialytic Membrane Induced by Complexation toward Dendritic Receptors

        ACS Omega 2021, 23, 15514-15522 DOI:10.1021/acsomega.1c02142

• Hartman T., Reisnerová M., Chudoba J., Svobodová E., Archipowa N., Kutta R. J., Cibulka R.:
  Photocatalytic Oxidative [2+2] Cycloelimination Reactions with Flavinium Salts: Mechanistic Study and Influence of the Catalyst Structure
  ChemPlusChem 2021, 86, 373–386. DOI: 10.1002/cplu.202000767
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• Edlová, T.; Čubiňák, M.; Tobrman, T.: 
  Cross-Coupling Reactions of Double or Triple Electrophilic Templates for Alkene Synthesis. 
  Synthesis 2021, 53, 255-266. DOI: 10.1055/s-0040-1707270
  
  
• Koudelka, J.; Tobrman, T.:
  Synthesis of 2-Substituted Cyclobutanones by a Suzuki Reaction and Dephosphorylation Sequence
  Eur. J. Org. Chem. 2021, 3260-3269 DOI:10.1002/ejoc.202100464
  
  
• Edlova, T.; Dvorakova, H.; Eigner, V.; Tobrman, T.:
  Substrate-Controlled Regioselective Bromination of 1,2-Disubstituted Cyclobutenes: An Application in the Synthesis of 2,3-Disubstituted Cyclobutenones
  J. Org. Chem. 2021, 86, 5820-5831 DOI:10.1021/acs.joc.1c00261
  
  
• Shishkanova, T.; Stepankova, N.; Tlusty, M.; Tobrman, T.; Jurasek, B.; Kuchar, M.; Trchova, M.; Fitl, P.; Vrnata, M.:
  Electrochemically oxidized 15-crown-5 substituted thiophene and host-guest interaction with new psychoactive substances
  Electrochimica Acta 2021,  737, 137862 DOI:10.1016/j.electacta.2021.137862
  
  
• Skopalová H., Kozmík V., Šmahel M., Svoboda J., Pacherová O., Kohout M., Novotná, V.:
  Mesomorphic properties of non-symmetric bent-core liquid crystals with a lateral substituent in the apex position
  Liq. Cryst. 2021, 48, 1010-1024. https://doi.org/10.1080/02678292.2020.1836567
  
  
• Cigl M., Hampl F., Svoboda J., Podoliak N., Stulov S., Kohout M., Novotná V.:
  Laterally substituted biphenyl benzoates – synthesis and mesomorphic properties
  Liq. Cryst. 2021, 48, 526-536. https://doi.org/10.1080/02678292.2020.1794069
  
  
• Spálovská D., Paškan M., Jurásek B., Kuchař M., Kohout M., Setnička V.:
  Structural spectroscopic study of enantiomerically pure synthetic cathinones and their major metabolites
  New J. Chem. 2021, 45, 850. https://doi.org/10.1039/D0NJ05065B
  
  
• Wolrab D., Frühauf P., Kolderová N., Kohout M.:
  Strong cation- and zwitterion-exchange-type mixed-mode stationary phases for separation of pharmaceuticals and biogenic amines in different chromatographic modes
  J. Chromatogr. A 2021, 1635, 461751. https://doi.org/10.1016/j.chroma.2020.461751
  
  
• Linhart I., Hanzlíková I., Mráz J., Dušková Š., Tvrdíková M., Vachová H.:
  Novel aminoarylcysteine adducts in globin of rats dosed with naphthylamine and nitronaphthalene isomers. 
  Arch. Toxicol. 2021, 95, 79-89. doi: 10.1007/s00204-020-02907-y
  
  
• Marques M.M.; Beland F.A.; Lachenmeier D.W.; Phillips D.H.; Chung F.L.; Dorman D.C.; Elmore S.E.; Hammond S.K.; Krstev S.K.; Linhart I.; Long A.S.; Mandrioli D.; Ogawa K.; Pappas J.J.; Parra Morte J.M.; Talaska G.; Tang M.S.; Thakur N.; van Tongeren M.; Vineis P.:
  IARC Monographs Vol 128 group. Carcinogenicity of acrolein, crotonaldehyde, and arecoline. 
  Lancet Oncol. 2021, 22, 19-20. doi: 10.1016/S1470-2045(20)30727-0
  
  
• Jágerová, D.; Šmahel, M.; Poryvai, A.; Macháček, J.; Novotná, V.; Kohout, M.:
  Photosensitive bent-core liquid crystals with laterally substituted azobenzene unit. Crystals, 2021, 11, 1265.
  https://doi.org/10.3390/cryst11101265
  
  
• Shruthi, S.; Smahel, M.; Kohout, M.; Shanker, G.; Hegde, G.:
  Influence of linking units on the photo responsive studies of azobenzene liquid Crystals: Application in optical storage devices 
  J. Mol. Liq. 2021, 339, 116744 DOI:10.1016/j.molliq.2021.116744
  
  
• Karongo, R.; Ge, M.; Horak, J.; Gross, H.; Kohout, M.; Lindner, W.; Lämmerhofer, M.:
  Rapid enantioselective amino acid analysis by ultra-high performance liquid chromatography-mass spectrometry combining 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate derivatization with core-shell quinine carbamate anion exchanger separation. J. Chromatogr. Open, 2021, 1, 100004.
  https://doi.org/10.1016/j.jcoa.2021.100004
  
  
• Herciková, J.; Spálovská, D.; Frühauf, P.; Izák, P.; Lindner, W.; Kohout, M.:
  Design and synthesis of naphthalene-based chiral strong cations exchangers and their application for chiral separation of basic drugs. J. Sep. Sci., 2021, 44, 3348-3356. DOI: 10.1002/jssc.202100127
  

2020

• Poryvai A., Bubnov A., Kohout M.:
  Chiral Photoresponsive Liquid Crystalline Materials Derived from Cyanoazobenzene Central Core: Effect of UV Light Illumination on Mesomorphic Behavior
  Crystals 2020, 10, 1161. https://doi.org/10.3390/cryst10121161
  
  
• Skopalová H., Špaček P., Kozmík V., Svoboda J., Novotná V., Pociecha D., Kohout M.:
  The Role of Substitution in the Apex Position of the Bent-Core on Mesomorphic Properties of New Series of Liquid Crystalline Materials
  Crystals, 2020, 10, 735. https://doi.org/10.3390/cryst10090735
  
  
• Guselnikova O., Postnikov P., Kolská Z., Záruba K., Kohout M., Elashnikov R., Švorčík V., Lyutakov O.:
  Homochiral metal-organic frameworks functionalized SERS substrate for atto-molar enantio-selective detection
  Appl. Mater. Today 2020, 20, 100666. https://doi.org/10.1016/j.apmt.2020.100666
  
  
• Kolderová N., Jurásek B., Kuchař M., Lindner W., Kohout M.:
  Gradient supercritical fluid chromatography coupled to mass spectrometry with a gradient flow of make-up solvent for enantioseparation of cathinones
  J. Chromatogr. A 2020, 1625, 461286. https://doi.org/10.1016/j.chroma.2020.461286
  
  
• Šmahel M., Poryvai A., Xiang Y., Pociecha D., Troha T., Novotná V., Svoboda J., Kohout M.:
  Photosensitive bent-core nematic liquid crystals with various linking units in the side arms: Structure-properties relationships
  J. Mol. Liq. 2020, 306, 112743. https://doi.org/10.1016/j.molliq.2020.112743
  
  
• Cigl M., Jurok R., Hampl F., Svoboda J., Podoliak N., Novotná V.:
  Lateral substituted phenyl biphenylcarboxylates ‒ non-chiral analogues of ferroelectric liquid crystals
  Liq.  Cryst. 2020, 47, 768-776. https://doi.org/10.1080/02678292.2019.1679903
  
  
• Gaálová J., Yalcinkaya F., Cuřínová P., Kohout M., Yalcinkaya B., Koštejn M., Jirsák J., Stibor I., Bara J. E., Van der Bruggen B., Izák P.:
  Separation of racemic compound by nanofibrous composite membranes with chiral selector
  J. Membr. Sci. 2020, 596, 117728. https://doi.org/10.1016/j.memsci.2019.117728
  
  
• Otmar M., Gaálová J., Žitka J., Brožová L., Cuřínová P., Kohout M., Hovorka Š., Bara J. E., Van der Bruggen B., Jirsák J., Izák P.:
  Preparation of PSEBS membranes bearing (S)-(-)-methylbenzylamine as chiral selector
  Eur. Polym. J. 2020, 122, 109381. https://doi.org/10.1016/j.eurpolymj.2019.109381
  
  
• Oeser, P.; Koudelka, J.; Dvořáková, H.; Tobrman, T.:
  Formation of trisubstituted buta-1,3-dienes and α,β-unsaturated ketones via the reaction of functionalized vinyl phosphates and vinyl phosphordiamidates with organometallic reagents.
  RSC Adv. 2020, 10, 35109-35120. DOI: 10.1039/D0RA07472A
  
  
• Čubiňák, M.; Tobrman, T.:
  Room-Temperature Negishi Reaction of Trisubstituted Vinyl Phosphates for the Synthesis of Tetrasubstituted Alkenes.
  J. Org. Chem. 2020, 85, 10728-10739. DOI: 10.1021/acs.joc.0c01254
  
  
• Polák, P.; Čejka, J.; Tobrman, T.:
  Formal Transition-Metal-Catalyzed Phosphole C–H Activation for the Synthesis of Pentasubstituted Phospholes.
  Org. Lett. 2020, 22, 2187─2190 DOI: 10.1021/acs.orglett.0c00359
  
  
• Tobrman, T; Krupička, M.; Polák, P.; Dvořáková, H.; Čubiňák, M.; Babor, M.; Dvořák, D.:
  Diastereoselective Cyclopropanation through Michael Addition‐Initiated Ring Closure between α,α‐Dibromoketones and α,β‐Unsaturated Fischer Carbene Complexes.
  Eur. J. Org. Chem. 2020, 429─436 DOI: 10.1002/ejoc.201901503
  
  
• Guricová, M.; Tobrman, T.; Pižl, M.; Žižková, S.; Hoskovcová, I.; Dvořák, D.:
  Synthesis, characterisation and electrochemical properties of Cr(0) aminocarbene complexes containing condensed heteroaromatic moiety.
  Organomet. Chem. 2020, 905, 121023 DOI: 10.1016/j.jorganchem.2019.121023

• Kortus, D.; Kundrat, O.; Tlusty, M.; Cejka, J.; Dvorakova, H.; Lhotak, P.:
  Inherent chirality through a simple dialkylation of 2,14-dithiacalix[4]arene
  New J. Chem. 2020, 44, 14496-14504 DOI:10.1039/d0nj03468a
  
  
• Tlusty, M.; Spalovska, D.; Kohout, M.; Eigner, V.; Lhotak, P.:
  Ketone transformation as a pathway to inherently chiral rigidified calix[4]arenes
  Chem. Commun. 2020, 56, 12773-12776 DOI:10.1039/d0cc05352j
  
  
• Kolarikova, V.; Rybackova, M.; Svoboda, M.; Kvicala, J.:
  Ring-closing metathesis of prochiral oxaenediynes to racemic 4-alkenyl-2-alkynyl-3,6-dihydro-2H-pyrans
  Beilstein J. Org. Chem.  2020, 16, 2757–2768 DOI:10.3762/bjoc.16.226
  
  
• Simunek, O.; Rybackova, M.; Svoboda, M.; Kvicala, J.:
  Synthesis, catalytic activity and medium fluorous recycle of fluorous analogues of PEPPSI catalysts
  J. Fluorine Chem. 2020, 236, 109588 DOI:10.1016/j.jfluchem.2020.109588
  
  
• Graml, A.; Neveselý, T.; Kutta, R.-J.; Cibulka, R.; König, B.:
  Deazaflavin reductive photocatalysis involves excited semiquinone radicals
  Nature Comm. 2020, 11, 3174.  DOI: 10.1038/s41467-020-16909-y
  
  
• Landovsky, T.; Eigner, V.; Babor, M.; Tichotova, M.; Dvorakova, H.; Lhotak, P.:
  Regioselective S_NAr reaction of the phenoxathiin-based thiacalixarene as a route to a novel macrocyclic skeleton
  Chem. Commun. 2020, 56, 78-81 DOI:10.1039/c9cc08335a
  
  
• Tlusty, M.; Dvorakova, H.; Cejka, J.; Kohout, M.; Lhotak, P.:
  Regioselective formation of the quinazoline moiety on the upper rim of calix[4]arene as a route to inherently chiral systems
  New J. Chem. 2020, 44, 6490-6500 DOI:10.1039/d0nj01035a
  
  
• Máková, V.; Holubová, B.; Tetour, D.; Brus, J.; Řezanka, M.; Rysová, M.; Hodačová, J.: 
  (1S,2S)‐Cyclohexane‐1,2‐diamine‐based Organosilane Fibres as a Powerful Tool Against Pathogenic Bacteria
  Polymers 2020, 12, 206 DOI:10.3390/polym12010206
  
  
• Cibulka, R.:
  Strong chemical reducing agents produced by light
  Nature 2020, 580, 31-32 DOI: 10.1038/d41586-020-00872-1
  
  
• Tolba, A. H.; Vávra, F.; Chudoba, J.; Cibulka, R.:
  Tuning flavin-based photocatalytic systems for application in the mild chemoselective aerobic oxidation of benzylic substrates
  Eur. J. Org. Chem. 2020, 1579–1585 DOI:10.1002/ejoc.201901628 Special issue Photochemical synthesis

• Schlosser J., Cibulka R., Groß P., Ihmels H., Mohrschladt C. J.:
  Visible-light induced di-π-methane rearrangement of dibenzobarrelene derivatives
  ChemPhotoChem 2020, 4, 132-137 DOI: 10.1002/cptc.201900221
  
  
• Zelenka, J.; Cibulka, R.; Roithová, J.:
  Flavinium catalyzed photooxidation: Detection and characterization of elusive peroxyflavinium intermediates
  Angew. Chem. Int. Ed. 2020, 58, 15412-15420 DOI: 10.1002/anie.201906293
  COVER:
  
  
  
• Mráz J., Hanzlíková I., Dušková Š., Tvrdíková M., Linhart I.:
  N-(2-Hydroxyethyl)-l-valyl-l-leucine: a novel urinary biomarker of ethylene oxide exposure in humans. 
  Toxicol Lett. 2020, 15, 18-22. doi: 10.1016/j.toxlet.2020.03.004
  
  
  

2019

• Slavik, P.; Krupicka, M.; Eigner, V.; Vrzal, L.; Dvorakova, H.; Lhotak, P.:
  Rearrangement of meta-Bridged Calix[4]arenes Promoted by Internal Strain
  J. Org. Chem. 2019, 84, 4229-4235, DOI:10.1021/acs.joc.9b00107
  
  
• Kortus, D.; Miksatko, J.; Kundrat, O.;  Babor, M.; Eigner, V.; Dvorakova, H.; Lhotak, P.:
  Chemistry of 2,14-Dithiacalix[4]arene: Alkylation and Conformational Behavior of Peralkylated Products
  J. Org. Chem. 2019, 84, 11572-11580, DOI:10.1021/acs.joc.9b01493
  
  
• Tlusty, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhotak, P.:
  Synthesis of Upper Rim-double-bridged Calix[4]​arenes bearing Seven Membered Rings and Related Compounds
  RSC Advances 2019, 9, 22017-22030 DOI:10.1039/c9ra05075b
  
  
  
• Pokluda, A.; Kohout, M.; Chudoba, J.; Krupička, M.; Cibulka, R.:
  Nitrosobenzene – Reagent for the Mitsunobu Esterification Reaction
  ACS Omega 2019, 4, 5012-5018. DOI: 10.1021/acsomega.8b03551
  
  
• Valenta, L.; Kovaricek, P.; Vales, V.; Bastl, Z.; Drogowska, K. A.; Verhagen, T. A.; Cibulka, R.; Kalbac, M.:
  Spatially resolved covalent functionalization patterns on graphene
  Angew. Chem. Int. Ed. 2019, 58, 1324-1328 DOI: 10.1002/anie.201810119
  
  
• Zelenka, J.; Svobodová, E.; Tarábek, J.; Hoskovcová, I.; Boguschová, V.; Bailly, S.; Sikorski, M.; Roithová, J.; Cibulka, R.:
  Combining flavin photocatalysis and organocatalysis: metal-free aerobic oxidation of unactivated benzylic substrates
  Org. Lett. 2019, 21, 114-119 DOI: 10.1021/acs.orglett.8b03547
  Highly cited paper (WOS)
  
  
• Jing, H.; Xu, M.; Xiang, Y.; Wang, E.; Liu, D.; Poryvai, A.; Kohout, M.; Éber, N.; Buka, A.:
  Light tunable gratings based on flexoelectric effect in photoresponsive bent-core nematics.
  Adv. Opt. Mater. 2019, 1801790 DOI: 10.1002/adom.201801790
  
  
• Pokluda, A.; Kohout, M.; Chudoba, J.; Krupička, M.; Cibulka, R.:
  Nitrosobenzene: Reagent for the Mitsunobu esterification reaction.
  ACS Omega 2019, 4, 5012-5018 DOI: 10.1021/acsomega.8b03551
  
  
• Spálovská, D.; Maříková, T.; Kohout, M.; Králík, F.; Kuchař, M.; Setnička, V.:
  Methylone and pentylone: Structural analysis of new psychoactive substances.
  Forensic Toxicol. 2019, 37, 366-377 DOI: 10.1007/s11419-019-00468-z
  
  
• Poryvai, A.; Bubnov, A.; Pociecha, D.; Svoboda, J.; Kohout, M.:
  The effect of the length of terminal n-alkyl carboxylate chain of self-assembling and photosensitive properties of chiral lactic acid derivatives.
  J. Mol. Liq. 2019, 275, 829-838 DOI: 10.1016/j.molliq.2018.11.058
  
  
• Geibel, C.; Dittrich, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; Lämmerhofer, M.:
  Evaluation of superficially porous particle based zwitterionic chiral ion exchangers against fully porous particle benchmarks for enantioselective ultra-high performance liquid chromatography.
  J. Chromatogr. A 2019, 1603, 130-140 DOI: 10.1016/j.chroma.2019.06.026
  
  
• Poryvai, A.; Vojtylová-Jurkovičová, T.; Šmahel, M.; Kolderová, N.; Tomášková, P.; Sýkora, D.; Kohout, M.:
  Determination of optical purity of lactic acid-based chiral liquid crystals and corresponding building blocks by chiral high-performance liquid chromatography and supercritical fluid chromatography.
  Molecules 2019, 24, 1099 DOI: 10.3390/molecules24061099
  
  
• Tlustý, M.; Eigner, V.; Babor, M.; Kohout, M.; Lhoták, P.:
  Synthesis of upper rim-double-bridged calix[4]arenes bearing seven membered rings and related compounds.
  RSC Adv. 2019, 9, 22017-22030. DOI: 10.1039/C9RA05075B
  
  
• Mráz J., Hanzlíková I., Linhart I., Dušková Š., Dabrowská L., Hejl K.:
  N-(2-Hydroxyethyl)-L-valyl-L-leucine in rat urine as a hydrolytic cleavage product of ethylene oxide adduct with globin.
  Arch Toxicol. 2019, 93, 603-613. doi: 10.1007/s00204-019-02388-8
  
  
• Linhart, I.:
  Chemická legislativa pohledem laboratorního chemika. 
  Chemické listy 2019, 113, 140-148.

2018

• Jurásek, B.; Králík, F.; Rimpelová S.; Čejka, J.; Setnička, V.; Ruml, T.; Kuchař, M.; Kohout, M.:
  Synthesis, Absolute Configuration and in vitro Cytotoxicity of Deschloroketamine Enantiomers: Rediscovered and Abused Dissociative Anaesthetic
  New. J. Chem. 2018, 42, 19360-19368 DOI: 10.1039/c8nj03107j
  COVER:
  
  
• Landovsky, T.; Dvorakova, H.; Eigner, V.; Babor, M.; Krupicka, M.; Kohout, M.; Lhotak, P.:
  Chemoselective Oxidation of Phenoxathiin-based Thiacalix[4]arene and the Stereoselective Alkylation of Products
  New J. Chem. 2018, 42, 20074-20086 DOI: 10.1039/C8NJ04690E
  
  
• Mojr, V.; Pitrova, G.; Strakova, K.; Prukala, D.; Brazevic, S.; Svobodová, E.; Hoskovcová, I.; Burdziński, G.; Slanina, T.; Sikorski, M.; Cibulka, R.: 
  Flavin Photocatalysts for  visible Light [2+2] Cycloadditions: Structure, Reactivity and Reaction Mechanism
  ChemCatChem 2018, 10, 849-858 DOI: 10.1002/cctc.201701490
  
  
• Marz, M.; Kohout, M.; Nevesely, T.; Chudoba, J.; Prukala, D.; Nizinski, S.; Sikorski, M.; Burdzinski, G.; Cibulka, R.:
  Azodicarboxylate-free esterification with triphenylphosphine mediated by flavin and visible light: method development and stereoselectivity control
  Org. Biomol. Chem. 2018, 16, 6809-6817 DOI:10.1039/C8OB01822G
  
  
• Mundil, R.; Sokolohorskyj, A.; Hosek, J.; Cvacka, J.; Cisarova, I.; Kvicala, J.; Merna, J.:
  Nickel and palladium complexes with fluorinated alkyl substituted α-diimine ligands for living/controlled olefin polymerization
  Polym. Chem. 2018, 9, 1234-1248 DOI: 10.1039/C8PY00201K
  
  
• Hosek, J.; Simunek, O.; Lipovska, P.; Kolarikova, V.; Kucnirova, K.; Edr, A.; Stepankova, N.; Rybackova, M.; Cvacka, J.; Kvicala, J.:
  Medium Fluorous Separation Using Hydrofluoroether and Weakly Polar Solvents for Environmentally Friendly Recycling of Catalysts
  ACS Sustainable Chem. Eng.  2018, 6, 7026-7034 DOI:10.1021/acssuschemeng.8b00865
  
  
• Kucnirova, K.; Simunek, O.; Rybackova, M.; Kvicala, J.:
  Structural Assignment of Fluorocyclobutenes by ¹⁹F NMR Spectroscopy – Comparison of Calculated ¹⁹F NMR Shielding Constants with Experimental ¹⁹F NMR Shifts
  Eur. J. Org. Chem. 2018, 3867-3874 DOI:10.1002/ejoc.201800482
  
  
• Slavik, P.; Eigner, V.; Lhotak, P.:
  meta-​Bridged calix[4]​arenes with the methylene moiety possessing in​/out stereochemistry of substituents
  New J. Chem. 2018 asap DOI:10.1039/c8nj02577k
  
  
• Landovsky, T.; Tichotova, M.; Vrzal, L.; Budka, J.; Eigner, V.; Dvorakova, H.; Lhotak, P.:
  Structure elucidation of phenoxathiin-​based thiacalix[4]​arene conformations using NOE and RDC data
  Tetrahedron 2018, 74, 902-907 DOI:10.1016/j.tet.2018.01.020
  
  
• Slavik, P.; Dvorakova, H.; Krupicka, M.; Lhotak, P.:
  Unexpected cleavage of upper rim-​bridged calix[4]​arenes leading to linear oligophenolic derivatives
  Org. Biomol. Chem. 2018, 59, 838-843 DOI:10.1039/C7OB03101G
  
  
• Slavik, P.; Lhotak, P.:
  Unusual reactivity of upper-​rim bridged calix[4]​arenes - Friedel-​Crafts alkylation via cleavage of the macrocyclic skeleton
  Tetrahedron 2018, 59, 1757-1759 DOI:10.1016/j.tetlet.2018.03.072
  
  

• Schmitt, K.; Woiwode, U.; Kohout, M.; Zhang, T.; Lindner, W.; Lämmerhofer, M.:
  Comparison of small size fully porous particles and superficially porous particles of chiral anion-exchange type stationary phases in ultra-high performance liquid chromatography: effect of particle and pore size on chromatographic efficiency and kinetic performance
  J. Chromatogr. A 2018, 1569, 149-159 DOI:10.1016/j.chroma.2018.07.056

• Spálovská, D.; Kralik, F.; Kohout, M.; Jurasek, B.; Habartová, L.; Kuchar, M.; Setnicka, V.: 
  Structure determination of butylone as a new psychoactive substance using chiroptical and vibrational spectroscopies 
  Chirality 2018, 30, 548-559 DOI:10.1002/chir.22825
  
  
• Wolrab, D.; Kohout, M.:
  Multimodální stacionární fáze pro kapalinovou chromatografii, způsob jejich přípravy a jejich použití.
  Národní patent č. 307339, číslo přihlášky 2017-193, datum udělení 2.5.2018, datum zveřejnění 13.6.2018.
  
  
• Kohout, M.; Wernisch, S.; Tuma, J.; Hettegger, H.; Picha, J.; Lindner W.: 
  Effect of different immobilization strategies on chiral recognition properties of Cinchona-based anion exchangers 
  J. Sep. Sci. 2018, 41, 1355-1364 DOI:10.1002/jssc.201701213
  
  
• Bajtai, A.; Fekete, B.; Palkó, M.; Fülöp, F.; Lindner, W.; Kohout, M.; Ilisz, I.; Péter, A.: 
  Comparative study on the liquid chromatographic enantioseparation of cyclic β-amino acids and the related cyclic β-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases 
  J. Sep. Sci. 2018, 41, 1216-1223 DOI:10.1002/jssc.201701190
  
  
• Sardella, R.; Macchiarulo, A.; Urbinati, F.; Ianni, F.; Carotti, A.; Kohout, M.; Lindner, W.; Péter, A.; Ilisz, I.: 
  Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers 
  J. Sep. Sci. 2018, 41, 1199-1207 DOI:10.1002/jssc.201701068
  
  
• Tuma, J.; Kohout, M.: 
  Silica gel-immobilized multidisciplinary materials applicable in stereoselective organocatalysis and HPLC separation 
  RSC Adv. 2018, 8, 1174-1181 DOI:10.1039/c7ra12658a
  
  
• Kozmik, V.; Rodinová, E.; Prausová, T.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Mesogens with central naphthalene core substituted at various positions 
  Liq. Cryst. 2018, 45, 744-756 DOI: 10.1080/02678292.2017.1380238
  
  
•  Bajzíková, K.; Vesely, J.; Kozmik, V.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Thiophene central core for the design of bent-shaped liquid crystals 
  J. Mol. Liq. 2018, 267, 496-503 DOI:10.1016/j.molliq.2018.02.009
  
  
• Horcic, M.; Svoboda, J.; Novotná, V.; Pociecha, D.; Gorecka, E.:
  Bent-core dimers with top-to-bottom linkage between central units 
  RSC Adv. 2018, 8, 22974-22985 DOI: 10.1039/c8ra04108c
  
  
• Mráz J, Hanzlíková I, Dušková Š, Tvrdíková M, Chrástecká H, Vajtrová R, Linhart I.:
  Determination of N-(2-hydroxyethyl)valine in globin of ethylene oxide-exposed workers using total acidic hydrolysis and HPLC-ESI-MS2
  Toxicol Lett. 2018, 298, 76-80. doi: 10.1016/j.toxlet.2018.06.1212

2017

• Maixner, J.; Jurásek, B.; Kohout, M.; Kuchar, M.; Kacer, P.:
  X-ray powder diffraction data for (S)-Deschloroketamine hydrochloride, C₁₃H₁₈ClNO.
  Powder Diffr. 2017, 32, 193-195. DOI:10.1017/S0885715617000586
  
  
• Bajzíková, K.; Svoboda, J.; Novotná, V.; Pociecha, D.; Gorecka E.:
  Bent-core mesogens with an aromatic unit at the terminal position
  New J. Chem. 2017, 41, 4672-4679 DOI: 10.1039/C6NJ03908A
  
  
• Žurek, J.; Svobodová, E.; Šturala, J.; Dvořáková, H.; Svoboda, J.; Cibulka, R.:
  Chiral ethylene-bridged flavinium salts: The stereoselectivity of flavin-10a-hydroperoxide formation and the effect of substitution on the photochemical properties
  Tetrahedron Asymmetry 2017, asap DOI:10.1016/j.tetasy.2017.10.029
  
  
• Muchová; E.; Bezek, M.; Suchan, J.; Cibulka, R.; Slavíček, P.:
  Molecular Dynamics and Metadynamics Simulations of [2+2] Photocycloaddition
  Int. J. Quantum Chem. 2017, asap DOI:10.1002/qua.25534
  
  
  
• Dobrovolny, K.; Ulbrich, P.; Svecova, M.; Rimpelova, S.; Malincik, J.; Kohout, M.; Svoboda, J.; Bartunek, V.: 
  Copper nanoparticles in glycerol-​polyvinyl alcohol matrix: In situ preparation, stabilization and antimicrobial activity
  Journal of Alloys and Compounds 2017, 697, 147-155 DOI:10.1016/j.jallcom.2016.12.144
  
  
• Kolderova, N.; Nevesely, T.; Sturala, J.; Kuchar, M.; Holakovsky, R.; Kohout, M.:
  Enantioseparation of chiral sulfoxides on amylose-​based columns: comparison of normal phase liquid chromatography and supercritical fluid chromatography
  Chromatographia 2017, 80, 547-557 DOI: 10.1007/s10337-016-3234-6
  
  
• Kohout, M.; Alaasar, M.; Poryvai, A.; Novotna, V.; Poppe, S.; Tschierske, C.; Svoboda, J.: 
  Photosensitive bent-​core liquid crystals based on methyl substituted 3-​hydroxybenzoic acid
  RSC Advances 2017, 7, 35805-35813 DOI:10.1039/C7RA05632J
  
  
• Wolrab, D.; Fruehauf, P.; Gerner, C.; Kohout, M.; Lindner, W.: 
  Consequences of transition from liquid chromatography to supercritical fluid chromatography on the overall performance of a chiral zwitterionic ion-​exchanger
  Journal of Chromatography A 2017, 1517, 165-175 DOI:10.1016/j.chroma.2017.08.022
  
  
• Pallova, L.; Kozmik, V.; Kohout, M.; Svoboda, J.; Novotna, V.; Pociecha, D.: 
  Bent-​core liquid crystals with a 2-​substituted 3-​hydroxybenzoic acid central core
  Liquid Crystals 2017, 44, 1306-1315 DOI: 10.1080/02678292.2016.1276981
  
  
• Zidkova, M.; Linhart, I.; Balikova, M.; Himl, M.; Dvorackova, V.; Lhotkova, E.; Palenicek, T.: 
  Identification of three new phase II metabolites of a designer drug methylone formed in rats by N-​demethylation followed by conjugation with dicarboxylic acids
  Xenobiotica 2017, asap DOI: 10.1080/00498254.2017.1349964
  
  
• Linhart, I.; Hanzlikova, I.; Mraz, J.; Duskova, S.:
  S-​(3-​Aminobenzanthron-​2-​yl)​cysteine in the globin of rats as a novel type of adduct and possible biomarker of exposure to 3-​nitrobenzanthrone, a potent environmental carcinogen
  Archives of Toxicology 2017, asap DOI:10.1007/s00204-017-1943-8
  
  
• Polak, P.; Dvorak, D.; Tobrman, T.:
  Cyanogen: A Versatile Reagent for Diversity-​Oriented Synthesis
  Synthesis 2017, 49, 1757-1766 DOI:10.1055/s-0036-1588410
  
  
• Polak, P.; Tobrman, T.:
  The synthesis of polysubstituted indoles from 3-​bromo-​2-​indolyl phosphates
  Org. Biomol. Chem. 2017, 15, 6233-6241 DOI:10.1039/C7OB01127J
  
  
• Polak, P.; Tobrman, T.:
  Dearomatization Strategy for the Synthesis of Arylated 2H-​Pyrroles and 2,​3,​5-​Trisubstituted 1H-​Pyrroles
  Org. Lett. 2017, 19, 460-4611 DOI: 10.1021/acs.orglett.7b02219
  
  
• Simunkova, N.; Tobrman, T.; Eigner, V.; Dvorak, D.:
  A Study on the Intramolecular Mitsunobu Reaction of N6-(ω-hydroxyalkyl)adenines
  J. Heterocyclic Chem 2017, asap DOI: 10.1002/jhet.2982
  
  
• Bregier, F.; Hudecek, O.; Chaux, F.; Penouilh, M.; Chambron, J.; Lhotak, P.; Aubert, E.; Espinosa, E.:
  Generation of Cryptophanes in Water by Disulfide Bridge Formation
  Eur. J. Org. Chem. 2017, 3795-3811 DOI:10.1002/ejoc.201700537
  
  
• Tlusty, M.; Slavik, P.; Kohout, M.; Eigner, V.; Lhotak, P.:
  Inherently Chiral Upper-Rim-Bridged Calix[4]arenes Possessing a Seven Membered Ring
  Org. Lett. 2017, 19, 2933-2936 DOI:10.1021/acs.orglett.7b01170
  
  
• Jirasek, M.; Strakova, K.; Nevesely, T.; Svobodova, E.; Rottnerova, Z.; Cibulka, R.:
  Flavin-mediated visible light [2+2] photocycloaddition of nitrogen and sulfur-containing dienes 
  Eur. J. Org. Chem. 2017, 2139-2146 DOI:10.1002/ejoc.201601377
  
  
• Slavik, P.; Eigner, V.; Bohm, S.; Lhotak, P.:
  Mercuration of Calix[4]arene Immobilized in the 1,2- and 1,3-Alternate Conformations
  Tetrahedron Letters 2017, 58, 1846-1850 DOI:10.1016/j.tetlet.2017.03.085
  
  
• Miksatko, J.; Eigner, V.; Kohout, M.; Lhotak, P.:
  Regio-/stereoselective Formation of Monosulfoxides from Thiacalix[4]arenes in All Possible Conformations
  Tetrahedron Letters 2017, 58, 1687-1691 DOI:10.1016/j.tetlet.2017.03.043
  
  
• März, M.; Chudoba, J.; Kohout, M.; Cibulka, R.:
  Photocatalytic Esterification under Mitsunobu Reaction Conditions Mediated by Flavin and Visible Light
  Org. Biomol. Chem. 2017, 15, 1970-1975 DOI:10.1039/C6OB02770A
  
  
• Spackova, J.; Svobodova, E.; Hartman, T.; Stibor, I.; Kopecka, J.; Cibulkova, J.; Chudoba, J.; Cibulka, R.:
  Visible light light [2+2] Photocycloaddition mediated by flavin derivative immobilized on mesoporous silica 
  ChemCatChem. 2017, 9, 1177-1181 DOI:10.1002/cctc.201601654
  
  
• Horčic, M.; Kohout, M.; Svoboda, J.; Novotna, V.; Pociecha, D.; Gorecka, E.:
  Core-to-core Dimers Forming Switchable Mesophase
  Chem.  Commun. 2017, 53, 2721-2724 DOI:10.1039/C6CC09983A
  
  
• Tlusty, M.; Slavik, P.; Dvorakova, H.; Eigner, V.; Lhotak, P.:
  Synthesis and Study of Calix[4]arenes bearing Azo Moieties at the meta Position
  Tetrahedron 2017, 73, 1230-1237 DOI:10.1016/j.tet.2017.01.025
  
  
• Rezankova, M.; Budka, J.; Miksatko, J.; Eigner, V.; Cisarova, I.; Curinova, P.; Lhotak, P.:
  Anion Receptors based on Intramolecularly Bridged Calix[4]arenes bearing Ureido Functions
  Tetrahedron 2017, 73, 742–749 DOI:10.1016/j.tet.2016.12.054

2016

• Bajzikova, K.; Kohout, M.; Tarabek, J.; Svoboda, J.; Novotna, V.; Vejpravova, J.; Pociecha, D.; Gorecka, E.:
  All-organic liquid crystalline radicals with a spin unit in the outer position of a bent-core system
  J. Mater. Chem. C 2016, 4, 11540-11547 DOI:10.1039/C6TC04346A
  
  
• Zidkova, M.; Linhart, I.; Balikova, M.; Himl, M.; Vana, L.; Vetyska, M.; Palenicek, T.; Lhotkova, E.; Dusek, M.:
  Study on metamolism of 5,6-methylenedioxy-2-aminoindane (MDAI) in rats: identification of urinary metabolites
  Xenobiotica 2016, asap DOI:10.1080/00498254.2016.1199919
  
  
• Vanova, H.; Tobrman, T.; Hoskovcova, I.; Dvorak, D.:
  Modular synthesis of Fischer biscarbene complexes of chromium
  Organometallics 2016, 35, 2999-3006 DOI:10.1021/acs.organomet.6b00527
  
  
• Mraz, J.; Hanzlikova, I.; Duskova, S.; Dabrowska, L.; Chrastecka, H.; Vajtrova, R.; Linhart, I.:
  Biological fate of styrene oxide adducts with globin: Elimination of cleavage products in the rat urine
  Toxicology Letters 2016, 261, 26-31 DOI:10.1016/j.toxlet.2016.08.022
  
  
• Lipovska, P.; Rathouska, L.; Simunek, O.; Hosek, J.; Kolarikova, V.; Rybackova, M.; Cvacka, J.; Svoboda, M.; Kvicala, J.:
  Synthesis and catalytic activity of ruthenium complexes modified with chiral racemic per- and polyfluorooxaalkanoates
  J. Fluorine Chem. 2016, 191, 14-22 DOI:10.1016/j.jfluchem.2016.09.005
  
  
• Kotek, V.; Polák, P.; Dvořáková, H.; Tobrman, T.:
  Aluminium Chloride Promoted Cross-Coupling of Trisubstituted Enol Phosphates with Organozinc Reagents En Route to the Stereoselective Synthesis of Tamoxifen and Its Analogues
  Eur. J. Org. Chem. 2016, 5037-5044 DOI:10.1002/ejoc.201600959
  
  
• Tůma, J.; Kohout, M.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Bent-core liquid crystals based on 6-substituted 3-hydroxybenzoic acid: the role of substitution and linkage group orientation on mesomorphic properties
  Liq. Cryst. 2016, 43, 1889-1900 DOI:10.1080/02678292.2016.1230789
  
  
• Slavik, P.; Eigner, V.; Lhotak, P.:
  A General Method for Obtaining Calixarene Derivatives in the 1,2-Alternate Conformation
  Tetrahedron 2016, 72, 6348-6355 DOI:10.1016/j.tet.2016.08.028
  
  
• Liska, A.; Lhotak, P.; Ludvik, J.:
  Electrochemical Reduction and Intramolecular Electron  Communication of Nitro Substituted Thiacalix[4]arene
  Electroanalysis 2016, 28, 2861-2865 DOI:10.1002/elan.201600342
  
  
• Klejch, T.; Slavicek, J.; Hudecek, O.; Eigner, V.; Gutierrez, N. A.; Curinova, P.; Lhotak, P.:
  Calix[4]arene Containing a Ureido Functionality on the Lower Rim as Highly Efficient Receptors for Anion Recognition
  New J. Chem. 2016, 40, 7935-7942 DOI:10.1039/c6nj01271j
  
  
• Kohout, M.; Vandenbussche, J.; Roller, A.; Tůma, J.; Boqaerts, J.; Bultinck, P.; Herrebout, W.; Lindner, W.:
  Absolute configuration of the antimalarial erythro-mefloquine - vibrational dichroism and X-ray diffraction studies of mefloquine and its thiourea derivative
  RSC Advances 2016, 6, 81461-81465 DOI:10.1039/C6RA19367F 
  
  
• Polak, P.; Vanova, H.; Dvorak, D.; Tobrman, T.:
  Recent Progress in Transition Metal-Catalyzed Stereoselective Synthesis of Acyclic All-Carbon Tetrasubstituted Alkenes
  Tetrahedron Lett. 2016, 57, 3684-3693 DOI:10.1016/j.tetlet.2016.07.030
  
  
• Navratil, R.; Tarabek, J.; Linhart, I.; Martinů, T.:
  Radical and Nitrenoid Reactivity of 3-Halo-3-phenyldiazirines
  Org. Lett. 2016, 18, 3734–3737 DOI:10.1021/acs.orglett.6b01753
  
  
• Miksatko, J.; Eigner, V.; Dvorakova, H.; Lhotak, P.:
  Selective Oxidation of Thiacalix[4]arene (cone) to all Corresponding Sulfoxides
  Tetrahedron Lett. 2016, 57, 3781–3784 DOI:10.1016/j.tetlet.2016.07.022
  
  
• Hartman, T.; Cibulka, R.:
  Photocatalytic systems with flavinium salts: From photolyase models to synthetic tool for cyclobutane ring opening 
  Org. Lett. 2016, 18, 3710-3713 DOI:10.1021/acs.orglett.6b01743
  
  
• Bím, D.; Svobodová, E.; Eigner, V.; Rulíšek, L.; Hodačová, J.:
  Copper(II) and Zinc(II) Complexes of Conformationally Constrained Polyazamacrocycles as Efficient Catalysts for RNA Model Substrate Cleavage in Aqueous Solution at Physiological pH
  Chem.  Eur. J. 2016, 22, 10426-10437 DOI:10.1002/chem.201601175
  
  

• Kohout, M.; Bubnov, A.; Šťurala, J.; Novotná, V.; Svoboda, J.:
  Effect on alkyl chain length in the terminal ester group on mesomorphic properties of new chiral lactic acid derivatives
  Liq. Cryst. 2016, 43, 1472-1485 DOI:10.1080/02678292.2016.1185170
  
  
• Grecsó, N.; Kohout, M.; Carotti, A.; Sardella, R.; Natalini, B.; Fülöp, F.; Lindner, W.; Péter, A.; Ilisz, I.: 
  Mechanistic considerations of enantiorecognition on novel Cinchona alkaloid-based zwitterionic chiral stationary phases from the aspect of the separation of trans-paroxetine enantiomers as model compounds
  J. Pharm. Biomed. Anal. 2016, 124, 164-173 DOI:10.1016/j.jpba.2016.02.043
  
  
• Wolrab, D.; Frühauf, P.; Moulisova, A.; Kuchar, M.; Gerner, C.; Lindner, W.; Kohout, M.:
  Chiral separation of new designer drugs (Cathinones) on chiral ion-exchange type stationary phases
  J. Pharm. Biomed. Anal. 2016, 120, 306-315 DOI:10.1016/j.jpba.2015.12.023
  
  

• Slavik, P.; Eigner, V.; Lhotak, P.:
  Shaping of Calix[4]arenes via Double Bridging of the Upper Rim
  Cryst. Eng. Comm. 2016, 18, 4964-4970 DOI:10.1039/C6CE00314A
  
  

• Neveselý, T.; Svobodová, E.; Chudoba, J.; Sikorski, M.; Cibulka, R.:
  Efficient metal-free aerobic photooxidation of sulfides to sulfoxides mediated by a vitamin B2 derivative and visible light 
  Adv. Synth. Catal. 2016, 358, 1654-1663 DOI:10.1002/adsc.201501123
  
  
• Mraz, J.; Hanzlikova, I.; Moulisova, A.; Duskova, S.; Hejl, K.; Bednarova, A.; Dabrowska, L.; Linhart, I.:
  Hydrolytic cleavage products of globin adducts in urine as possible biomarkers of cumulative dose: Proof of concept using styrene oxide as a model adduct-forming compound
  Chem. Res. Toxicol. 2016, 29, 676-686 DOI:10.1021/acs.chemrestox.5b00518
  
  
• Dolenský, B.; Kvíčala, J.; Paleta, O.:
  Methyl fluoroalkanoate as methyl-​transferring reagent. Unexpected participation of BAl2 (SN2) mechanism in the reaction of methyl 2,​3,​3,​3-​tetrafluoro-​2-​methoxypropanoate with amines.
  J. Fluorine Chem. 2016, 185, 31-35. DOI:10.1016/j.jfluchem.2016.02.012
  
  
• Kundrat, O.; Slavik, P.; Miksatko, J.:
  Introducing an Amine Group to Calix[5]arene: Comparison of Several Methods
  Supramol. Chem. 2016, 28, 450-454, DOI:10.1080/10610278.2015.1119275
  
  
• Tůma, J.; Kohout, M.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core - Part II
  Liq. Cryst. 2016, 43, 547-563, DOI: 10.1080/02678292.2015.1125535
  
  
• Kotek, V.; Polák, P.; Tobrman, T.:
  Efficient and Simple Preparation of Functionalized 1,1-Dibromoenol Phosphates
  Monatshefte fuer Chemie 2016, 147, 405-412, DOI: 10.1007/s00706-015-1613-6
  
  
• Linhart, I.; Himl, M.; Zidkova, M.; Balikova, M.; Lhotakova, E.; Palenicek, T.: 
  Metabolic Profile of Mephedrone: Identification of Normephedrone Conjugates with Dicarboxylic Acids as a New Type of Xenobiotic Phase II Metabolites
  Toxicology Letters 2016, 240, 114-121, DOI: 10.1016/j.toxlet.2015.10.025
  
  
• Botha, F.; Eigner, V.; Dvorakova, H.; Lhotak, P.: 
  Arylation of Thiacalix[4]arenes using Organomercurial Intermediates 
  New J. Chem. 2016,  40, 1104-1110, DOI:10.1039/C5NJ02427G + cover picture
  
  
• Slavik, P.; Kohout, M.; Böhm, S.; Eigner, V.; Lhotak, P.:
  Synthesis of Inherently Chiral Calixarenes via Direct Mercuration of the Partial Cone Conformation
  Chem. Commun. 2016, 52, 2366-2369 DOI:10.1039/C5CC09388K
  
  
• Stejskal, F.; Curinova, P.; Lhotak, P.:
  Unexpected Formation of Disulfide-based Biscalix[4]arenes
  Tetrahedron 2016, 72, 760-766 DOI:10.1016/j.tet.2015.12.037
   

2015

• Kotek, V.; Dvořáková, H.; Tobrman, T.:
  Modular and Highly Stereoselective Approach to All-Carbon Tetrasubstituted Alkenes
  Org. Lett. 2015, 17, 608-611. DOI: 10.1021/ol503624v
  
  
• Hartman, T.; Šturala, J.; Cibulka, R.:
  Two-phase Oxidations with Aqueous Hydrogen Peroxide Catalysed by Amphiphilic Pyridinium and Diazinium Salts
  Adv. Synth. Catal. 2015, 357, 3573-3586. DOI:10.1002/adsc.201500687 
  
  
• Kolaříková, V.; Šimůnek, O.; Rybáčková, M.; Cvačka, J.; Březinová, A.; Kvíčala, J.:
  Transition Metal Complexes Bearing NHC Ligands with Secondary Polyfluoroalkyl Groups
  J. Chem. Soc., Dalton Trans. 2015, 44, 19663-19673. DOI:10.1039/C5DT02258D
  
  
• Králík, A.; Linhart, I.; Váňa, L.; Moulisová, A.:
  Identification of New DNA Adducts of Phenylnitrenium
  Chem. Res. Toxicol. 2015, 28, 1317-1325. DOI:10.1021/acs.chemrestox.5b00120
  
  
• Kozmík, V.; Poznik, M.; Svoboda, J.; Frere, P.:
  Dithieno[3,2-b:2 ',3 '-d]furan as a New Building Block for Fused Conjugated Systems
  Tetrahedron Lett. 2015, 56, 6251-6253. DOI:10.1016/j.tetlet.2015.09.107
  
  
• Nunes, S.; Bürglová, K.; Hodačová, J.; Ferreira, R.; Carlos, L.; Almeida, P.; Cattoën, X.; Man, M.; Bermudez, V.:
  Nanostructuring of Bridged Organosilane Precursors with Pendant Alkyl Chains
  Eur. J. Org. Chem. 2015, 1218-1225. DOI:10.1002/ejic.201402673
  
  
• Zajicova, M.; Eigner, V.; Budka, J.; Lhotak, P.:
  Intramolecular Bridging of Calix[4]arene Dialdoximes
  Tetrahedron Lett. 2015, 56, 5529–5532 DOI:10.1016/j.tetlet.2015.08.032 
   
• Vrzal, L.; Kratochvilova-Simanova, M.; Landovsky, T.; Polivkova, K.; Budka, J.; Dvorakova, H.; Lhotak, P.:
  Application of RDC Enhanced NMR Spectroscopy in Structural Analysis of Thiacalix[4]arene Derivatives
  Org. Biomol. Chem. 2015, 13, 9610-9618 DOI:10.1039/C5OB01424G
  
  
• Stejskal, F.; Eigner, V.; Dvorakova, H.; Curinova, P.; Lhotak, P.:
  Direct C-H Azidation of Calix[4]arene as a Novel Method to Access meta Substituted Derivatives
  Tetrahedron Lett. 2015, 56, 5357-5361 DOI:10.1016/j.tetlet.2015.08.002
  
  
• Slavik, P.; Eigner, V.; Lhotak, P.:
  Intramolecularly Bridged Calix[4]arenes with Pronounced Complexation Ability toward Neutral Compounds
  Org. Lett. 2015, 17, 2788-2791 DOI:10.1021/acs.orglett.5b01200
  
  
• Liska, A.; Flidrova, K.; Lhotak, P.; Ludvik, J.:
  Influence of Structure on Electrochemical Reduction of Isomeric Mono- and Di-, Nitro- or Nitrosocalix[4]arenes
  Monatshefte fuer Chemie 2015, 146, 857-862 DOI:10.1007/s00706-015-1441-8
  
  
• Hucko, M.; Dvorakova, H.; Eigner, V.; Lhotak, P.:
  2,14-Dithiacalix[4]arene and its Homooxa Analogues: Synthesis and Dynamic NMR Study of Conformational Behaviour
  Chem. Comm. 2015, 51, 7051-7053 DOI:10.1039/C5CC00819K
  
  
• Spendlikova, I.; John, J.; Cuba, V.; Jirasek, J.;  Lhotak, P.:
  Thiacalixarenes: Radiation Stability and Eu/Am Extraction in Synergistic Systems with COSANs
  J. Radioanalyt. Nucl. Chem. 2015, 304, 257-262 DOI:10.1007/s10967-014-3694-9
  
  
• Mackova, M.; Miksatko, J.; Budka, J.; Eigner, V.; Curinova, P.; Lhotak, P.:
  Chiral Anion Recognition by a Ureido-Thiacalix[4]arene Ligand Immobilized in the 1,3-Alternate Conformation
  New J. Chem. 2015, 39, 1382-1389 DOI:10.1039/C4NJ01956C
  
  
• Flidrova, K.; Liska, A.; Ludvik, J.; Eigner, V.; Lhotak, P.:
  Fullerene Recognition by 5-Nitro-11,17,23,29-tetramethylcalix[5]arene
  Tetrahedron Lett. 2015, 56, 1535-1538 DOI:10.1016/j.tetlet.2015.02.016
  
  
• Skacel, J.; Budka, J.; Eigner, V.; Lhotak, P.:
  Regioselective Friedel-Crafts Acylation of Calix[4]arenes
  Tetrahedron 2015, 71, 1959-1965 DOI:10.1016/j.tet.2015.02.021
  
  
• Trišović, N.; Antanasijević, J.; Tóth-Katona, T.; Kohout, M.; Salamonczyk, M.; Sprunt, S.; Jákli, A.; Fodor-Csorba, K.:
  Azo-containing asymmetric bent-core liquid crystals with modulated smectic phase
  RSC Adv. 2015, 5, 64886-64891. DOI: 10.1039/c5ra09764a
  
  

• Kohout, M.; Bielec, B.; Steindl, P.; Trettenhahn, G.; Lindner, W.:
  Mechanistic aspects of the direct C-acylation of cyclic 1,3-diones with various unactivated carboxylic acids
  Tetrahedron 2015, 71, 2698-2707. DOI: 10.1016/j.tet.2015.03.037
   
• von Koschitzky, I.; Gerhardt, H.; Lämmerhofer, M.; Kohout, M.; Gehringer, M.; Laufer, S.; Pink, M.; Schmitz-Spanke, S.; Strube, C.; Kaiser, A.:
  New insights into novel inhibitors against deoxyhypusine hydrolase from plasmodium falciparum: compounds with an iron chelating potential
  Amino Acids 2015, 47, 1155-1166. DOI: 10.1007/s00726-015-1943-z
   
• Kohout, M.; Kozmík, V.; Slabochová, M.; Tůma, J.; Svoboda, J.; Novotná, V.; Pociecha, D.:
  Bent-shaped liquid crystals based on 4-substituted 3-hydroxybenzoic acid central core
  Liq. Cryst. 2015, 42, 87-103. DOI: 10.1080/02678292.2014.965232
   
• Moulisová, A.; Linhart, I.: 
  Preparation of cysteine adducts by regioselective ring-opening reactions of phenyloxirane
  Heterocyclic Commun. 2015, 21, 61-65 DOI:10.1515/hc-2015-0042
  
  
• Rybáčková, M.; Hošek, J.; Šimůnek, O.; Kolaříková, V.; Kvíčala, J.:
  Computational study of productive and non-productive cycles in fluoroalkene metathesis. 
  Beilstein J. Org. Chem. 2015, 11, 2150–2157. DOI:10.3762/bjoc.11.232
  
  
• Hošek, J.; Rybáčková, M.; Čejka, J.; Cvačka, J.; Kvíčala, J.:  
  Synthesis of heavy Fluorous Ruthenium Metathesis catalysts using the stereoselective addition of polyfluoroalkyllithium to sterically hindered diimines.
  Organometallics 2015, 34(13), 3327-3334. DOI:10.1021/acs.organomet.5b00325
  
  

• Křováček M., Dvořák D.:
  Synthesis of potentially biologically active 6-(1,3-butadiynyl)purines.
  J. Heterocyclic Chem. 2015, 52, 40-47 DOI:10.1002/jhet.1938
  
  
• Bousa, D.; Jankovsky, O.; Sedmidubsky, D.; Luxa, J.; Sturala, J.; Pumera, M.; Sofer, Z.:
  Mesomeric Effects of Graphene Modified with Diazonium Salts: Substituent Type and Position Influence its Properties
  Chem. Eur. J. 2015, 21, 17728-17738. DOI:10.1002/chem.201502127
  
  
• Tomanová P., Šturala J., Buděšínský M., Cibulka R.:
  A click chemistry approach towards flavin-cyclodextrin conjugates – bioinspired sulfoxidation catalysts,
  Molecules 2015, 20, 19837-19848. DOI:10.3390/molecules201119667
  
  
• Holakovský R., März M., Cibulka R.:
  Urea derivatives based on a 1,1'-binaphthalene skeleton as chiral solvating agents for sulfoxides,
  Tetrahedron: Asymmetry 2015, 26, 1328-1334. DOI:10.1016/j.tetasy.2015.10.011
  
  
• Mojr V., Svobodová E., Straková K., Neveselý T., Chudoba J., Dvořáková H., Cibulka R.:
  Tailoring Flavins for Visible Light Photocatalysis: Organocatalytic [2+2] Cycloadditions Mediated by a Flavin Derivative and Visible Light,
  Chem. Comm. 2015, 51, 12036 – 12039. DOI:10.1039/C5CC01344E
  
  
• Sofer, Z.; Jankovský, O.; Šimek, P.; Sedmidubský, D.; Šturala, J.; Kosina, J.; Mikšová, R.; Macková, A.; Mikulics, M.; Pumera, M.:
  Insight into the Mechanism of the Thermal Reduction of Graphite Oxide: Deuterium-Labeled Graphite Oxide Is the Key,
  ACS Nano 2015, 9, 5478-5485. DOI:10.1021/acsnano.5b01463
  
  
• Šturala J., Boháčová S., Chudoba J., Metelková R., Cibulka R.:
  Electron-deficient Heteroarenium salts – an Organocatalytic Tool for Activation of Hydrogen Peroxide in Oxidations,
  J. Org. Chem. 2015, 80, 2676-2699. DOI:10.1021/jo502865f
  
  
• Cibulka, R.:
  Artificial flavin systems for chemoselective and stereoselective oxidations (Microreview),
  Eur. J. Org. Chem. 2015, 915-932. DOI:10.1002/ejoc.201403275 + Cover picture