Publications

Hývl, J.; Roithová, J. Mass Spectrometric Studies of Reductive Elimination from Pd(IV) Complexes. Organic Letters 2014, 16 (1), 200-203 DOI: 10.1021/ol403190g.

Ye, S.; Kupper, C.; Meyer, S.; Andris, E.; Navrátil, R.; Krahe, O.; Mondal, B.; Atanasov, M.; Bill, E.; Roithová, J.; et al. Magnetic Circular Dichroism Evidence for an Unusual Electronic Structure of a Tetracarbene–Oxoiron(IV) Complex. Journal of the American Chemical Society 2016, 138 (43), 14312-14325 DOI: 10.1021/jacs.6b07708.

Kadlcikova, A.; Valterová, I.; Ducháčková, L.; Roithová, J.; Kotora, M. Lewis Base Catalyzed Enantioselective Allylation of α,β-Unsaturated Aldehydes. Chemistry - A European Journal 2010, 16 (31), 9442-9445 DOI: 10.1002/chem.201001523.

Riedl, J.; Pohl, R.; Ernsting, N. P.; Orság, P.; Fojta, M.; Hocek, M. Labelling of nucleosides and oligonucleotides by solvatochromic 4-aminophthalimide fluorophore for studying DNA–protein interactions. Chemical Science 2012, 3 (9), 2797 DOI: 10.1039/c2sc20404e.

Albiñana, C. Berenguer; Machara, A.; Řezáčová, P.; Pachl, P.; Konvalinka, J.; Kožíšek, M. Kinetic, thermodynamic and structural analysis of tamiphosphor binding to neuraminidase of H1N1 (2009) pandemic influenza. European Journal of Medicinal Chemistry 2016, 121, 100-109 DOI: 10.1016/j.ejmech.2016.05.016.

Císařová, I.; Jacko, J.; Kotora, M.; Rulíšek, L.; Staś, M. Ir-Catalyzed Cycloaddition of Tribenzocyclyne with Biphenylenes. Journal of Organic Chemistry 2022, 87 (1), 744-750.

Schulz, J.; Shcherbachenko, E.; Roithová, J. Investigation of Geminally Diaurated Arene Complexes in the Gas Phase. Organometallics 2015, 34 (16), 3979-3987 DOI: 10.1021/acs.organomet.5b00343.

Škríba, A.; Jašík, J.; Andris, E.; Roithová, J. Interaction of Ruthenium(II) with Terminal Alkynes: Benchmarking DFT Methods with Spectroscopic Data. Organometallics 2016, 35 (7), 990-994 DOI: 10.1021/acs.organomet.6b00021.

Jašík, J.; Roithová, J. Infrared spectroscopy of CHCl2+ molecular dications. International Journal of Mass Spectrometry 2015, 377, 109-115 DOI: 10.1016/j.ijms.2014.07.001.

Jašík, J.; Navrátil, R.; Němec, I.; Roithová, J. Infrared and Visible Photodissociation Spectra of Rhodamine Ions at 3 K in the Gas Phase. The Journal of Physical Chemistry A 2015, 119 (51), 12648-12655 DOI: 10.1021/acs.jpca.5b08462.

Řezanka, P.; Rokosová, L.; Řezanková, K.; Bláhová, M.; Řezanka, M.; Sýkora, D.; Jindřich, J.; Král, V. The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.

Řezanka, P.; Rokosová, L.; Řezanková, K.; Bláhová, M.; Řezanka, M.; Sýkora, D.; Jindřich, J.; Král, V. The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.

Řezanka, P.; Rokosová, L.; Řezanková, K.; Bláhová, M.; Řezanka, M.; Sýkora, D.; Jindřich, J.; Král, V. The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.

Řezanka, P.; Rokosová, L.; Řezanková, K.; Bláhová, M.; Řezanka, M.; Sýkora, D.; Jindřich, J.; Král, V. The influence of the substituent position in monocarboxymethyl-γ-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2014, 37 (19), 2779-2784 DOI: 10.1002/jssc.201400604.

Řezanka, P.; Řezanková, K.; Sedláčková, H.; Mašek, J.; Rokosová, L.; Bláhová, M.; Řezanka, M.; Jindřich, J.; Sýkora, D.; Král, V. Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.

Řezanka, P.; Řezanková, K.; Sedláčková, H.; Mašek, J.; Rokosová, L.; Bláhová, M.; Řezanka, M.; Jindřich, J.; Sýkora, D.; Král, V. Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.

Řezanka, P.; Řezanková, K.; Sedláčková, H.; Mašek, J.; Rokosová, L.; Bláhová, M.; Řezanka, M.; Jindřich, J.; Sýkora, D.; Král, V. Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.

Řezanka, P.; Řezanková, K.; Sedláčková, H.; Mašek, J.; Rokosová, L.; Bláhová, M.; Řezanka, M.; Jindřich, J.; Sýkora, D.; Král, V. Influence of substituent position and cavity size of the regioisomers of monocarboxymethyl-α-, β-, and γ-cyclodextrins on the apparent stability constants of their complexes with both enantiomers of Tröger's base. Journal of Separation Science 2016, 39 (5), 980-985 DOI: 10.1002/jssc.201500845.

Raindlová, V.; Janoušková, M.; Slavíčková, M.; Perlíková, P.; Boháčová, S.; Milisavljevič, N.; Šanderová, H.; Benda, M.; Barvík, I.; Krásný, L.; et al. Influence of major-groove chemical modifications of DNA on transcription by bacterial RNA polymerases. Nucleic Acids Research 2016, 44 (7), 3000-3012 DOI: 10.1093/nar/gkw171.

Řezanka, M.; Řezanka, P.; Sýkora, D.; Jindřich, J.; Král, V. Impact of substituent position in monosubstituted α-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2012, 35 (7), 811–815 DOI: 10.1002/jssc.201101034.

Řezanka, M.; Řezanka, P.; Sýkora, D.; Jindřich, J.; Král, V. Impact of substituent position in monosubstituted α-cyclodextrins on enantioselectivity in capillary electrophoresis. Journal of Separation Science 2012, 35 (7), 811–815 DOI: 10.1002/jssc.201101034.

Valero, G.; Schimer, J.; Císařová, I.; Vesely, J.; Moyano, A.; Rios, R. Highly enantioselective organocatalytic synthesis of piperidines. Formal synthesis of (−)-Paroxetine. Tetrahedron Letters 2009, 50 (17), 1943-1946 DOI: 10.1016/j.tetlet.2009.02.049.

Remeš, M.; Vesely, J. Highly Enantioselective Organocatalytic Formation of Functionalized Cyclopentane Derivatives via Tandem Conjugate Addition/α-Alkylation of Enals. European Journal of Organic Chemistry 2012, 2012 (20), 3747-3752 DOI: 10.1002/ejoc.201200334.

Číhalová, S.; Valero, G.; Schimer, J.; Humpl, M.; Dračínský, M.; Moyano, A.; Rios, R.; Vesely, J. Highly enantioselective organocatalytic cascade reaction for the synthesis of piperidines and oxazolidines. Tetrahedron 2011, 67 (46), 8942-8950 DOI: 10.1016/j.tet.2011.08.079.

Companyó, X.; Hejnová, M.; Kamlar, M.; Vesely, J.; Moyano, A.; Rios, R. Highly enantioselective fluoromalonate addition to α,β-unsaturated aldehydes. Tetrahedron Letters 2009, 50 (35), 5021-5024 DOI: 10.1016/j.tetlet.2009.06.092.