Department of Organic Chemistry - Publications

Publications of our authors:

2021

• 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
  
  
• 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

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:
  
  

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

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
  
  
  

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