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Publikace našich autorů

 

2017

  • 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 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. 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. 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

  • 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. 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,
    J. Org. Chem. 2015, 80, 2676-2699. DOI:10.1021/jo502865f

  • Cibulka, R.:
    Artificial flavin systems for chemoselective and stereoselective oxidations (Microreview),
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Aktualizováno: 20.9.2017 17:55, Autor: Ondřej Kundrát

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