Publikácie
  1. Salem OM, Vilková M, Janočková J, Jendželovský R, Fedoročko P, Žilecká E, et al. New spiro tria(thia)zolidine-acridines as topoisomerase inhibitors, DNA binders and cytostatic compounds. Int J Biol Macromol 2016;86:690-700.
  2. Takacsová M, Čonková M, Martinková M, Gonda J. Convenient approach to an advanced intermediate for salinosporamide A synthesis. Tetrahedron Asymmetry 2016;27(7-8):369-376.
  3. Očenášová L, Kutschy P, Gonda J, Pilátová M, Gönciová G, Mojžiš J, et al. Synthesis of new 5-bromo derivatives of indole and spiroindole phytoalexins. Chem Pap 2016;70(5):635-648.
  4. Cisáriková A, Barbieriková Z, Janovec L, Imrich J, Hunáková L, Bačová Z, et al. Acridin-3,6-dialkyldithiourea hydrochlorides as new photosensitizers for photodynamic therapy of mouse leukemia cells. Bioorg Med Chem 2016;24(9):2011-2022.
  5. Martinková M, Gonda J. Marine cytotoxic jaspine B and its stereoisomers: Biological activity and syntheses. Carbohydr Res 2016;423:1-42.
  6. Imrich J, Sabolová D, Vilková M, KudláČová J. Unexpected regiospecific formation and DNA binding of new 3-(acridin-9-yl)methyl-2-iminothiazolidin-4-ones. J Chem Sci 2016;128(2):269-277.
  7. Stanková K, Martinková M, Gonda J, Bago M, Pilátová M, Gönciová G. The convergent total synthesis of cytotoxic homospisulosine and its 3-epi-analogue. Tetrahedron Asymmetry 2015;26(24):1394-1407.
  8. Garcia-Calderon M, Pons-Ferrer T, Mrazova A, Pal'ove-Balang P, Vilkova M, Perez-Delgado CM, et al. Modulation of phenolic metabolism under stress conditions in a lotus japonicus mutant lacking plastidic glutamine synthetase. Front Plant Sci 2015;6.
  9. Salem O, Vilkova M, Plsikova J, Grolmusova A, Burikova M, Prokaiova M, et al. DNA binding, anti-tumour activity and reactivity toward cell thiols of acridin-9-ylalkenoic derivatives. J Chem Sci 2015;127(5):931-940.
  10. Matejova M, Janovec L, Imrich J. Study of the synthesis of novel trisubstituted acridines. Arkivoc 2015;2015(5):134-152.
  11. Martinková M, Mezeiová E, Fabišíková M, Gonda J, Pilátová M, Mojžiš J. Total synthesis of pachastrissamine together with its 4-epi-congener via [3,3]-sigmatropic rearrangements and antiproliferative/cytotoxic evaluation Dedicated to Associated Professor Ladislav Kniežo on the occasion of his 70th birthday. Carbohydr Res 2015;402:6-24.
  12. Budovská M, Kudličková Z, Kutschy P, Pilátová M, Mojžiš J. A facile method for the synthesis of indole phytoalexin rutalexin. Tetrahedron Lett 2015;56(25):3945-3947.
  13. Ungvarská Maľučká L, Vilková M, Kožíšek J, Imrich J. Strong deshielding in aromatic isoxazolines. Magn Reson Chem 2015.
  14. Krajnakova L, Paulikova H, Bacova Z, Bakos J, Janovec L, Imrich J, et al. Intracellular distribution of 3,6-bis(3-alkylguanidino)acridines determines their cytotoxicity. Neoplasma 2015;62(1):98-107.
  15. Elečková L, Balogh IS, Imrich J, Andruch V. Application of cinnamoyl derivative as a new ligand for dispersive liquid-liquid microextraction and spectrophotometric determination of cobalt. J Anal Chem 2015;70(3):298-304.
  16. Pacheco-Torres J, Mukherjee N, Walko M, López-Larrubia P, Ballesteros P, Cerdan S, et al. Image guided drug release from pH-sensitive Ion channel-functionalized stealth liposomes into an in vivo glioblastoma model. Nanomed Nanotechnol Biol Med 2015;11(6):1345-1354.
  17. Vilková M, Ungvarská Maľučká L, Imrich J. Prediction by 13C NMR of regioselectivity in 1,3-dipolar cycloadditions of acridin-9-yl dipolarophiles. Magn Reson Chem 2015.
  18. Rostášová I, Vilková M, Vargová Z, Walko M, Almáši M, Imrich J, et al. Dipeptide interactions with Zn(II)-cyclen artificial model for molecular recognition. J Mol Recogn 2015;28(4):211-219.
  19. Malinak D, Gonda J, Korabecny J, Dolezal R, Honegr J, Soukup O, Očenášová, L., Györyová, K. A review of the total synthesis of (+)-lactacystin and its analogs. Curr Org Chem 2015;19(20):1980-2001.
  20. Almáši M, Vargová Z, Sabolová D, Kudláčová J, Hudecová D, Kuchár J, et al. Ag(I) and Zn(II) isonicotinate complexes: Design, characterization, antimicrobial effect, and CT-DNA binding studies. J Coord Chem 2015;68(24):4423-4443.
  21. Čižeková L, Grolmusová A, Ipóthová Z, Barbieriková Z, Brezová V, Hunáková L, Imrich J, Janovec L, Dovinová I, Paulikocá H. Novel 3,6-bis(imidazolidine)acridines as effective photosensitizers for photodynamic therapy. Bioorganic and Medicinal Chemistry. 2014;22(17):4684-93.
  22. Salayová A, Kudličková Z, Baláž M, Budovská M, Pilátová M, Mojžiš J, Monde K, Petrovaj J, Gondova T. Stereoselective synthesis of 1-methoxyspiroindoline phytoalexins and their amino analogues. Tetrahedron Asymmetry. 2014.
  23. Martinková M, Mezeiová E, Gonda J, Jacková D, Pomikalová K. Total synthesis of (-)-jaspine B and its 4-epi-analogue from d-xylose. Tetrahedron Asymmetry. 2014;25(9):750-66.
  24. Vilková M, Prokaiová M, Imrich J. Spontaneous cyclization of (acridin-9-ylmethyl)thioureas to spiro [dihydroacridine-9′(10′H),5-imidazolidine]-2-thiones, a novel type of acridine spirocycles. Tetrahedron. 2014;70(4):944-61.
  25. Budovská M. A novel palladium-catalyzed cyclization of indole phytoalexin brassinin and its 1-substituted derivatives. RSC Advances. 2014;4(11):5575-82.
  26. Kello M, Drutovic D, Chripkova M, Pilatova M, Budovska M, Kulikova L, Urdzik P, Mojzis J. ROS-dependent antiproliferative effect of brassinin derivative homobrassinin in human colorectal cancer Caco2 cells. Molecules. 2014;19(8):10877-97.
  27. Hamulakova S, Janovec L, Hrabinova M, Spilovska K, Korabecny J, Kristian P, Kuca K, Imrich J. Synthesis and biological evaluation of novel tacrine derivatives and tacrine-coumarin hybrids as cholinesterase inhibitors. J Med Chem. 2014;57(16):7073-84.
  28. Hamulakova S, Imrich J, Janovec L, Kristian P, Danihel I, Holas O, Pohanka M, Bohm S, Kožurková M, Kuča K.. Novel tacrine/acridine anticholinesterase inhibitors with piperazine and thiourea linkers. Int J Biol Macromol. 2014;70:435-9.
  29. Chripkova M, Drutovic D, Pilatova M, Mikes J, Budovska M, Vaskova J, Broggini M, Mirossay L, Mojzis J. Brassinin and its derivatives as potential anticancer agents. Toxicology in Vitro. 2014;28(5):909-15.
  30. Ungvarsky J, Plsikova J, Janovec L, Koval J, Mikes J, Mikesová L, Harvanova, D., Fedorocko, P., Kristian, P., Kasparkova, J., Brabec, V., Vojtickova, M., Sabolova, D., Stramova, Z., Rosocha, J., Imrich, J., Kozurkova, M. Novel trisubstituted acridines as human telomeric quadruplex binding ligands. Bioorg Chem. 2014;57:13-29.
  31. Baláž P, Baláž M, Čaplovičová M, Zorkovská A, Čaplovič ̗, Psotka M. The dual role of sulfur-containing amino acids in the synthesis of IV-VI semiconductor nanocrystals: A mechanochemical approach. Faraday Discuss 2014;170:169-179.
  32. Gonda J, Maliňák D, Kováčová M, Martinková M. A convenient approach to an advanced intermediate for (+)-lactacystin synthesis. Tetrahedron Lett. 2013;54(49):6768-71.
  33. Gonda J, Maliňák D, Kováčová M, Martinková M, Walko M. A diastereoselective C-C bond formation at C-5 of d-gulose. A convenient approach to (5S)-5-C-alkyl-β-l-lyxo-hexofuranoses. Tetrahedron Asymmetry. 2013.
  34. Ipóthová Z, Paulíková H, Čižeková L, Hunáková Ľ, Labudová M, Grolmusová A, et al. Subcellular localization of proflavine derivative and induction of oxidative stress - in vitro studies. Bioorganic and Medicinal Chemistry. 2013;21(21):6726-31.
  35. Budovská M, Pilátová M, Varinská L, Mojžiš J, Mezencev R. The synthesis and anticancer activity of analogs of the indole phytoalexins brassinin, 1-methoxyspirobrassinol methyl ether and cyclobrassinin this work is dedicated to the memory of associated professor peter kutschy (1953-2012). Bioorganic and Medicinal Chemistry. 2013;21(21):6623-33.
  36. Špaková Raschmanová J, Martinková M, Gonda J, Uhríková A. Stereoselective total synthesis of protected sulfamisterin and its analogues. Chemical Papers. 2013;67(10):1317-29.
  37. Martinková M, Pomikalová K, Gonda J, Vilková M. A common approach to the total synthesis of l-arabino-, l-ribo-C 18-phytosphingosines, ent-2-epi-jaspine B and 3-epi-jaspine B from d-mannose. Tetrahedron. 2013;69(38):8228-44.
  38. Očenáš P, Tomášová L, Kutschy P, Pazdera P, Mojžiš J, Pilátová M. Spirocyclisation of phytoalexin 1-methoxybrassinin in the presence of grignard reagents. Chemical Papers. 2013;67(6):631-42.
  39. Petrul'ová-Poracká V, Repčák M, Vilková M, Imrich J. Coumarins of matricaria chamomilla L.: Aglycones and glycosides. Food Chem. 2013;141(1):54-9.
  40. Vuong QV, Siposova K, Nguyen TT, Antosova A, Balogova L, Drajna L, et al. Binding of glyco-acridine derivatives to lysozyme leads to inhibition of amyloid fibrillization. Biomacromolecules. 2013;14(4):1035-43.
  41. Pilatova M, Ivanova L, Kutschy P, Varinska L, Saxunova L, Repovska M, et al. In vitro toxicity of camalexin derivatives in human cancer and non-cancer cells. Toxicology in Vitro. 2013;27(2):939-44.
  42. Martinková M, Gonda J, Uhríková A, Raschmanová JŠ, Vilková M, Oroszová B. A stereoselective total synthesis of the HCl salts of mycestericins F, G and ent-F. Tetrahedron Asymmetry. 2013;24(2-3):121-33.
  43. Budovská M, Kutschy P, Kožár T, Gondová T, Petrovaj J. Synthesis of spiroindoline phytoalexin (S)-(-)-spirobrassinin and its unnatural (R)-(+)-enantiomer. Tetrahedron. 2013;69(3):1092-104.
  44. Gondová T, Petrovaj J, Kutschy P, Armstrong DW. Stereoselective separation of spiroindoline phytoalexins on R-naphthylethyl cyclofructan 6-based chiral stationary phase. Journal of Chromatography A. 2013;1272:100-5.
  45. Martinková M, Pomikalová K, Gonda J. Total synthesis of N,O,O,O-tetraacetyl-d-ribo-phytosphingosine and its 2-epi-congener. Chemical Papers. 2013;67(1):84-91.
  46. Seliga R, Pilatova M, Sarissky M, Viglasky V, Walko M, Mojzis J. Novel naphthalimide polyamine derivatives as potential antitumor agents. Mol Biol Rep. 2013;40(6):4129-37.
  47. Paulíková H, Vantová Z, Hunáková Ľ, Čižeková L, Čarná M, Kožurková M, et al. DNA binding acridine-thiazolidinone agents affecting intracellular glutathione. Bioorganic and Medicinal Chemistry. 2012;20(24):7139-48.
  48. Plsikova J, Janovec L, Koval J, Ungvarsky J, Mikes J, Jendzelovsky R, et al. 3,6-bis(3-alkylguanidino)acridines as DNA-intercalating antitumor agents. Eur J Med Chem. 2012;57:283-95.
  49. Hamulakova S, Janovec L, Hrabinova M, Kristian P, Kuca K, Banasova M, et al. Synthesis, design and biological evaluation of novel highly potent tacrine congeners for the treatment of alzheimer's disease. Eur J Med Chem. 2012;55:23-31.
  50. Martinková M, Gonda J, Uhríková A, Raschmanová JS, Kuchár J. An efficient synthesis of the polar part of sulfamisterin and its analogs. Carbohydr Res. 2012;352:23-36.
  51. Martinková M, Gonda J, Raschmanová JŠ, Kuchár J, Kožíšek J. A stereoselective synthesis of an α-substituted α-amino acid as a substructure for the construction of myriocin. Tetrahedron Asymmetry. 2012;23(8):536-46.
  52. Eliašová A, Poracká V, Pal'ove-Balang P, Imrich J, Repčák M. Accumulation of tetracoumaroyl spermine in matricaria chamomilla during floral development and nitrogen deficiency. Zeitschrift fur Naturforschung - Section C Journal of Biosciences. 2012;67(1-2):58-64.
  53. Gondová T, Petrovaj J, Kutschy P, Čurillová Z, Salayová A, Fabián M, et al. Enantioseparation of novel amino analogs of indole phytoalexins on macrocyclic glycopeptide-based chiral stationary phase. Chromatographia. 2011;74(11-12):751-7.
  54. Martinková M, Gonda J, Pomikalová K, Kožíšek J, Kuchár J. A facile synthesis of D-ribo-C 20-phytosphingosine and its C2 epimer from D-ribose. Carbohydr Res. 2011;346(13):1728-38.
  55. Martinková M, Gonda J, Uhríková A, Kovácová M. Stereoselective synthesis of the polar part of mycestericins E and G. Chemical Papers. 2011;65(4):527-35.
  56. Krajníková A, Gyepes R, Gyoryová K, Šubrt J, Imrich J. Preparation, crystal structure and spectroscopic properties of dimeric [zn(2-bromobenzoato) 2(phenazone)] 2 and monomeric [zn(2-bromobenzoato) 2(thiourea) 2]•2H 2O. J Chem Cryst. 2011;41(7):1036-43.
  57. Mezencev R, Updegrove T, Kutschy P, Repovská M, McDonald JF. Camalexin induces apoptosis in T-leukemia jurkat cells by increased concentration of reactive oxygen species and activation of caspase-8 and caspase-9. Journal of Natural Medicines. 2011;65(3-4):488-99.
  58. Antosova A, Chelli B, Bystrenova E, Siposova K, Valle F, Imrich J, et al. Structure-activity relationship of acridine derivatives to amyloid aggregation of lysozyme. Biochimica et Biophysica Acta - General Subjects. 2011;1810(4):465-74.
  59. Janovec L, Kožurková M, Sabolová D, Ungvarský J, Paulíková H, Plšíková J, et al. Cytotoxic 3,6-bis((imidazolidinone)imino)acridines: Synthesis, DNA binding and molecular modeling. Bioorganic and Medicinal Chemistry. 2011;19(5):1790-801.
  60. Gonda J, Martinková M, Baur A. A short stereoselective synthesis of the protected uracil 3′-epi-polyoxin C. Tetrahedron Asymmetry. 2011;22(2):207-14. 
  61. Vargová Z, Balentová E, Walko M, Arabuli L, Hermann P, Lukeš I. Amino acids binding to zn 2+-cyclen molecular receptor in aqueous solution. Journal of Molecular Recognition. 2011;24(2):295-302.
  62. Kozurkova M, Hamulakova S, Gazova Z, Paulikova H, Kristian P. Neuroactive multifunctional tacrine congeners with cholinesterase, anti-amyloid aggregation and neuroprotective properties. Pharmaceuticals. 2011;4(2):382-418.
  63. Martinková M, Gonda J, Raschmanová JS, Slaninková M, Kuchár J. Total synthesis of a protected form of sphingofungin e using the [3,3]-sigmatropic rearrangement of an allylic thiocyanate as the key reaction. Carbohydr Res. 2010;345(17):2427-37.
  64. Kutschy P, Sýkora A, Curillová Z, Repovská M, Pilátová M, Mojžiš J, et al. Glyoxyl analogs of indole phytoalexins: Synthesis and anticancer activity. Collect Czech Chem Commun. 2010;75(8):887-903.
  65. Klika KD, Budovská M, Kutschy P. Enantiodifferentiation of phytoalexin spirobrassinin derivatives using the chiral solvating agent (R)-(+)-1,1′-bi-2-naphthol in conjunction with molecular modeling. Tetrahedron Asymmetry. 2010;21(6):647-58.
  66. Klika KD, Budovská M, Kutschy P. NMR spectral enantioresolution of spirobrassinin and 1-methoxyspirobrassinin enantiomers using (S)-(-)-ethyl lactate and modeling of spirobrassinin self-association for rationalization of its self-induced diastereomeric anisochromism (SIDA) and enantiomer self-disproportionation on achiral-phase chromatography (ESDAC) phenomena. J Fluorine Chem. 2010;131(4):467-76.
  67. Bedlčoviová Z, Imrich J, Kristian P, Danihel I, Böhm S, Sabolová D, et al. Novel carbohydrazide and hydrazone biomarkers based on 9-substituted acridine and anthracene fluorogens. Heterocycles. 2010;80(2):1047-66.
  68. Potočák I, Imrich J, Danihel I, Koíšek J, Klika KD. 4-(9,10-dihydroacridin-9-ylidene)thio-semicarbazide and its five-membered thia-zole and six-membered thia-zine derivatives. Acta Crystallographica Section C: Crystal Structure Communications. 2010;66(2):o87-92.
  69. Imrich J, Tomaščková J, Danihel I, Kristian P, Böhm S, Klika KD. Selective formation of 5- or 6-membered rings, 1,3-thiazolidin-4-one vs. 1,3-thiazin-4-one, from acridine thiosemicarbazides by the use of ethyne acid esters. Heterocycles. 2010;80(1):489-503.
  70. Böhm S, Tomaščiková J, Imrich J, Danihel I, Kristian P, Koch A, et al. Computational study to assign structure, tautomerism, E/Z and s-cis/s-trans isomerism, π-delocalization, partial aromaticity, and the ring size of 1,3-thiazolidin-4-ones and 1,3-thiazin-4-ones formed from thiosemicarbazides. Journal of Molecular Structure: THEOCHEM. 2009;916(1-3):105-18.
  71. Mezencev R, Kutschy P, Salayova A, Updegrove T, Mcdonald JF. The design, synthesis and anticancer activity of new nitrogen mustard derivatives of natural indole phytoalexin 1-methoxyspirobrassinol. Neoplasma. 2009;56(4):321-30.
  72. Vantová Z, Paulíková H, Sabolová D, Kožurková M, Sucháňová M, Janovec L, et al. Cytotoxic activity of acridin-3,6-diyl dithiourea hydrochlorides in human leukemia line HL-60 and resistant subline HL-60/ADR. Int J Biol Macromol. 2009;45(2):174-80.
  73. Fröhlichová Z, Imrich J, Danihel I, Kristian P, Böhm S, Sabolová D, et al. Spectroscopic, structural and theoretical studies of novel, potentially cytotoxic 4-acridonecarboxamide imines. Spectrochimica Acta - Part A: Molecular and Biomolecular Spectroscopy. 2009;73(2):238-48.
  74. Kutschy P, Salayová A, Čurillová Z, Kožár T, Mezencev R, Mojžiš J, et al. 2-(substituted phenyl)amino analogs of 1-methoxyspirobrassinol methyl ether: Synthesis and anticancer activity. Bioorganic and Medicinal Chemistry. 2009;17(10):3698-712.
  75. Mezencev R, Galizzi M, Kutschy P, Docampo R. Trypanosoma cruzi: Antiproliferative effect of indole phytoalexins on intracellular amastigotes in vitro. Exp Parasitol. 2009;122(1):66-9.
  76. Fröhlichová Z, Tomaščikov J, Imrich J, Kristian P, Danihel I, Bhm S, et al. Synthesis and properties of novel biologically interesting polycyclic 1,3,4-oxadiazoles containing acridine/acridone moieties. Heterocycles. 2009;77(2):1019-35.
  77. Šeršeň F, Walko M, Loos D. Antioxidative effect of some hydroxy substituted aromatic bisimines. Gen Physiol Biophys. 2009;28(2):210-4.
  78. Martinková M, Gonda J, Raschmanová J, Novodomská A, Kožíšek J, Perasinová L. A novel synthetic approach to C-glycosyl-D- and L-alanines. Molecules. 2008;13(12):3171-83.
  79. Hamul'aková S, Kristian P, Jun D, Kuča K, Imrich J, Danihel I, et al. Synthesis, structure, and cholinergic effect of novel neuroprotective compounds bearing the tacrine pharmacophore. Heterocycles. 2008;76(2):1219-35.
  80. Gajdošíková E, Martinková M, Gonda J, Čonka P. Microwave accelerated aza-claisen rearrangement. Molecules. 2008;13(11):2837-47.
  81. Mezencev R, Kutschy P, Salayová A, Čurillová Z, Mojžiš J, Pilátová M, et al. Anticancer properties of 2-piperidyl analogues of the natural indole phytoalexin 1-methoxyspirobrassinol. Chemotherapy. 2008;54(5):372-8.
  82. Gazova Z, Bellova A, Daxnerova Z, Imrich J, Kristian P, Tomascikova J, et al. Acridine derivatives inhibit lysozyme aggregation. European Biophysics Journal. 2008;37(7):1261-70.
  83. Martinková M, Gonda J, Raschmanová J, Uhríková A. Stereoselective synthesis of both enantiomers of α-(hydroxymethyl)glutamic acid. Tetrahedron Asymmetry. 2008;19(16):1879-85.
  84. Kožurková M, Sabolová D, Janovec L, Mikeš J, Koval' J, Ungvarský J, et al. Cytotoxic activity of proflavine diureas: Synthesis, antitumor, evaluation and DNA binding properties of 1′,1″-(acridin-3,6-diyl)-3′,3″-dialkyldiureas. Bioorganic and Medicinal Chemistry. 2008;16(7):3976-84.
  85. Tomaščiková J, Danihel I, Böhm S, Imrich J, Kristian P, Potočňák I, et al. Molecular and solid-state structure of methyl [2-(acridin-9-ylimino)-3-(tert-butylamino)-4-oxothiazolidin-5-ylidene]ac etate. J Mol Struct. 2008;875(1-3):419-26.
  86. Tomaščiková J, Imrich J, Danihel I, Böhm S, Kristian P, Pisarčíková J, et al. Regioselectivity and tautomerism of novel five-membered ring nitrogen heterocycles formed via cyclocondensation of acylthiosemicarbazides. Molecules. 2008;13(3):501-18.
  87. Čurillová Z, Kutschy P, Solčániová E, Pilátová M, Mojžiš J, Kováčik V. Synthesis and antiproliferative activity of 1-methoxy-, 1-(α-D-ribofuranosyl)- and 1-(β-D-ribofuranosyl)brassenin B. Arkivoc. 2008;2008(8):85-104.
  88. Klok M, Walko M, Geertsema EM, Ruangsupapichat N, Kistemaker JCM, Meetsma A, et al. New mechanistic insight in the thermal helix inversion of second-generation molecular motors. Chemistry - A European Journal. 2008;14(35):11183-93.
  89. Sénéchal-David K, Zaman N, Walko M, Halza E, Rivière E, Guillot R, et al. Combining organic photochromism with inorganic paramagnetism-optical tuning of the iron(ii) electronic structure. Dalton Transactions. 2008(14):1932-6.
  90. Čurillová Z, Kutschy P, Budovská M, Nakahashi A, Monde K. Stereoselective synthesis of (R)-(+)-1-methoxyspirobrassinin, (2R,3R)-(-)-1-methoxyspirobrassinol methyl ether and their enantiomers or diastereoisomers. Tetrahedron Lett. 2007;48(46):8200-4.
  91. Martinková M, Gonda J, Raschmanová J, Vojtičková M. The efficient preparation of α-substituted serine scaffolds as the chiral building blocks for the synthesis of SPT inhibitors. Tetrahedron. 2007;63(43):10603-7.
  92. Janovec L, Böhm S, Danihel I, Imrich J, Kristian P, Klika KD. Theoretical confirmation of the reaction mechanism leading to regioselective formation of thiazolidin-4-one from bromoacetic acid derivatives. Collect Czech Chem Commun. 2007;72(10):1435-45.
  93. Kožurková M, Sabolová D, Paulíková H, Janovec L, Kristian P, Bajdichová M, et al. DNA binding properties and evaluation of cytotoxic activity of 9,10-bis-N-substituted (aminomethyl)anthracenes. Int J Biol Macromol. 2007;41(4):415-22.
  94. Gonda J, Martinková M, Zadrošová A, Šoteková M, Raschmanová J, Čonka P, et al. Microwave accelerated aza-claisen rearrangements. Tetrahedron Lett. 2007;48(39):6912-5.
  95. Tomaščiková J, Imrich J, Danihel I, Bǒhm S, Kristian P. Heterocyclization of (acridin-9-yl)thiosemicarbazides with dimethyl acetylenedicarboxylate. Collect Czech Chem Commun. 2007;72(3):347-62.
  96. Janovec L, Sabolová D, Kožurková M, Paulíková H, Kristian P, Ungvarský J, et al. Synthesis, DNA interaction, and cytotoxic activity of a novel proflavine-dithiazolidinone pharmacophore. Bioconjug Chem. 2007;18(1):93-100.
  97. Mendoza SM, Lubomska M, Walko M, Feringa BL, Rudolf P. Characterization by X-ray photoemission spectroscopy of the open and closed forms of a dithienylethene switch in thin films. Journal of Physical Chemistry C. 2007;111(44):16533-7.
  98. Koçer A, Walko M, Feringa BL. Synthesis and utilization of reversible and irreversible light-activated nanovalves derived from the channel protein MscL. Nature Protocols. 2007;2(6):1426-37.
  99. Walko M, Feringa BL. The isolation and photochemistry of individual atropisomers of photochromic diarylethenes. Chemical Communications. 2007(17):1745-7.
  100. Martinková M, Gonda J, Raschmanová J. Novel furanoid α-substitued α-amino acid as a potent turn mimic in peptide synthesis. Molecules. 2006;11(7):564-73.
  101. Martinková M, Gonda J, Džoganová M. A new stereocontrolled approach to a key intermediate in the synthesis of (25,3R)-capreomycidine. Collect Czech Chem Commun. 2006;71(8):1199-210.
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