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Department of Organic Chemistry - Publications

Publications of our authors:


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  202414, 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. 202420, 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. 202415, 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. 2024430, 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. 202489, 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, 4662-4671DOI: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

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  • 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
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  • 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.

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  • 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


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  • 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. h
    ttps://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. 2020596, 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. 2020122, 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 SNAr 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
    New. J. Chem. 2018, 42, 19360-19368 DOI: 10.1039/c8nj03107j

  • 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 2016240, 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. 201544, 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. 2015304, 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. 201511, 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

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    Synthesis of potentially biologically active 6-(1,3-butadiynyl)purines.
    J. Heterocyclic Chem. 2015, 52, 40-47 DOI:10.1002/jhet.1938

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    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. 201551, 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,
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Updated: 18.10.2024 16:05, Author: Jan Budka

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