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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.; 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.
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.
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.
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.
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.
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.
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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.
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.
Malkov, A. V.; Ramírez-López, P.; Bendová), L. Biedermann; Rulíšek, L.; Dufková, L.; Kotora, M.; Zhu, F.; Kočovský, P. On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosi lanes catalyzed by QUINOX, a chiral lsoquinoline N-oxide. Journal of the American Chemical Society 2008, 130 (15), 5341-5348 DOI: 10.1021/ja711338q.
Malkov, A. V.; Ramírez-López, P.; Bendová), L. Biedermann; Rulíšek, L.; Dufková, L.; Kotora, M.; Zhu, F.; Kočovský, P. On the mechanism of asymmetric allylation of aldehydes with allyltrichlorosi lanes catalyzed by QUINOX, a chiral lsoquinoline N-oxide. Journal of the American Chemical Society 2008, 130 (15), 5341-5348 DOI: 10.1021/ja711338q.
Fanfrlík, J.; Kolář, M.; Kamlar, M.; Hurný, D.; Ruiz, F. X.; Cousido-Siah, A.; Mitschler, A.; Řezáč, J.; Munusamy, E.; Lepšík, M.; et al. Modulation of Aldose Reductase Inhibition by Halogen Bond Tuning. ACS Chemical Biology 2013, 8 (11), 2484-2492 DOI: 10.1021/cb400526n.
Fanfrlík, J.; Kolář, M.; Kamlar, M.; Hurný, D.; Ruiz, F. X.; Cousido-Siah, A.; Mitschler, A.; Řezáč, J.; Munusamy, E.; Lepšík, M.; et al. Modulation of Aldose Reductase Inhibition by Halogen Bond Tuning. ACS Chemical Biology 2013, 8 (11), 2484-2492 DOI: 10.1021/cb400526n.
Škríba, A.; Schulz, J.; Roithová, J. Monitoring of Reaction Intermediates in the Gas Phase: Ruthenium-Catalyzed C–C Coupling. Organometallics 2014, 33 (23), 6868-6878 DOI: 10.1021/om500933w.
Anania, M.; Jašík, J.; Jašíková, L.; Roithová, J.; Shcherbachenko, E.; Zelenka, J. Monoaurated vs. diaurated intermediates: causality or independence?. Chemical Science 2020, 11 (4), 980-988 DOI: 10.1039/c9sc05662a.
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