Department of Organic Chemistry - Publications

Publications of our authors:

2025

• Burešová Z., Grygarová M., Prokopová E., Klikar M., Pytela O., Váňa J., Fahim M. A. M., Kanyashree J., Zubova E., Bartáček J., Tydlitát J., Růžičková Z., Cibulka R., Schanze K. S., Bureš F.: 
  Divergent photoreduction of nitroaromatic compounds catalysed by dithienoquinoxaline 
  J. Catal. 2025, accepted. DOI: 10.1016/j.jcat.2025.116033
  
  
• Koudelka, J., Tobrman, T.: 
  Three-component synthesis of β-sulfonyl enamines and dienamines enabled by silver(i) acetate
  RSC Adv. 2025, 15, 3602-3606, DOI: https://doi.org/10.1039/D4RA08480B
  
  
• Pavlovska T., Havlík M., Labíková M., Cibulka R.:
  Biomimetic Orthogonal Removal of Arylacyl Protecting Groupsfrom the C-Terminus of Substituted Amino Acids andOligopeptides via Flavin N(5)-iminium Covalent Adducts. 
  Adv. Synth. Catal. 2025, accepted. DOI: 10.1002/adsc.202401556
  
  
• Ledvinka, J., Rota Sperti, F., Paragi, G., Pirrotta, M., Chéron, N., Valverde, I. E., Menova, P.,  Monchaud D.:
  Fluorescence Detection of DNA/RNA G-Quadruplexes (G4s) by Twice-asSmart Ligands
  ChemMedChem 2025, e202400829, doi.org/10.1002/cmdc.202400829 
  
  
  
  

2024

• Ramírez-Cortés F., Ménová P.:  
  Hepatocyte targeting via the asialoglycoprotein receptor.
  RSC Med. Chem.  2024, Advance Article. DOI: https://doi.org/10.1039/D4MD00652F.
  
  
• Obertík R., Ludvíková L., Chudoba J., Cibulka R.:
  Chemoselective Anaerobic Dehydrogenation of Alcohols By Using Visible Light and a Positively Charged Deazaflavin Catalyst Regenerated by Acetonitrile Solvent.
  ChemCatChem  2024, accepted. DOI: 10.1002/cctc.202401795.
  
  
• 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.
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• 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, 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

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
  COVER:
  
  
  

• 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.:
  Mesomorphic properties of non-symmetric bent-core liquid crystals with a lateral substituent in the apex position
  Liq. Cryst. 2021, accepted. 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, accepted. 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

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
  
  
• 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

• 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, asap, DOI: 10.1021/acs.orglett.8b03547
  
  
• 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
  
  

• 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
  
  
• 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

• Slavik, P.; Eigner, V.; Lhotak, P.:
  A General Method for Obtaining Calixarene Derivatives in the 1,2-Alternate Conformation
  Tetrahedron 2016, 72, asap DOI:10.1016/j.tet.2016.08.028
  
  
• 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, asap DOI:10.1039/c6nj01271j
  
  
• Liska, A.; Lhotak, P.; Ludvik, J.:
  Electrochemical Reduction and Intramolecular Electron  Communication of Nitro Substituted Thiacalix[4]arene
  Electroanalysis 2016, asap DOI:10.1002/elan.201600342
  
  
• 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. Toxic. 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