Publications

Found 502 results
Author Title [ Type(Desc)] Year
Journal Article
Coufal, R.; Tošner, Z.; Drahoňovský, D.; Vohlídal, J. Hemiacetal-based dynamic systems: a new mechanistic insight. Organic and Biomolecular Chemistry 2023, 21 (34), 6956-6968.
Gülak, S.; Štěpánek, O.; Malberg, J.; Rad, B. Rezaei; Kotora, M.; Wolf, R.; von Wangelin, A. Jacobi. Highly chemoselective cobalt-catalyzed biaryl coupling reactions. Chem. Sci. 2013, 4 (2), 776-784 DOI: 10.1039/C2SC21667A.
Zhang, K.; Meazza, M.; Docekal, V.; Light, M. E.; Vesely, J.; Rios, R. Highly Diastereo- and Enantioselective Synthesis of alpha-Spiro-delta-lactams by an Organocascade Reaction. European Journal of Organic Chemistry 2017, No. 13, 1749-1756 DOI: 10.1002/ejoc.201700193.
Kamlar, M.; Bravo, N.; Alba, A. - N. R.; Hybelbauerová, S.; Císařová, I.; Vesely, J.; Moyano, A.; Rios, R. Highly Enantioselective Addition of 1-Fluoro-1-nitro(phenylsulfonyl)methane to α,β-Unsaturated Aldehydes. European Journal of Organic Chemistry 2010, 2010 (28), 5464-5470 DOI: 10.1002/ejoc.201000851.
Franc, M.; Urban, M.; Císařová, I.; Vesely, J. Highly enantioselective addition of sulfur-containing heterocycles to isatin-derived ketimines. Organic & Biomolecular Chemistry 2019, 17 (31), 7309-7314 DOI: 10.1039/c9ob01338e.
Číhalová, S.; RemesÌ, M.; Císařová, I.; Veselý, J. Highly Enantioselective Aza-Baylis–Hillman-Type Reaction of α,β-Unsaturated Aldehydes with In Situ Generated N -Boc- and N -Cbz-Imines. European Journal of Organic Chemistry 2009, 2009 (36), 6277-6280 DOI: 10.1002/ejoc.200900969.
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.
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.
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.
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.
Kamlar, M.; Vesely, J. Highly enantioselective organocatalytic α-selenylation of aldehydes using hypervalent iodine compounds. Tetrahedron: Asymmetry 2013, 24 (5-6), 254-259 DOI: 10.1016/j.tetasy.2013.02.008.
Bednářová, E.; Kotora, M.; Malatinec, Š.; Tanaka, H. Highly Enantioselective Ring-Opening of meso-Epoxides with O- and N-Nucleophiles Catalyzed by a Chiral Sc(III)/bipyridine Complex. European Journal of Organic Chemistry 2021, 2021 (8), 1249-1257.
Osifová, Z.; Šála, M.; Dračínský, M. Hydrogen-Bonding Interactions of 8-Substituted Purine Derivatives. ACS Omega 2023, 8 (28), 25538-25548.
Kugler, M.; Hadzima, M.; Dzijak, R.; Rampmaier, R.; Srb, P.; Vrzal, L.; Voburka, Z.; Majer, P.; Řezáčová, P.; Vrábel, M. Identification of specific carbonic anhydrase inhibitors via in situ click chemistry, phage-display and synthetic peptide libraries: comparison of the methods and structural study. RSC Medicinal Chemistry 2023, 14 (1), 144-153.
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.
Gálisová, A.; Groborz, O.; Hájek, M.; Hrubý, M.; Jirák, D.; Kolouchová, K.; Sedláček, O.; Sticová, E.; Švec, P.; Trousil, J.; et al. Implant-forming polymeric 19F MRI-tracer with tunable dissolution. Journal of Controlled Release 2020, 327 (November), 50-60 DOI: 10.1016/j.jconrel.2020.07.026.
Vesely, J.; Ledvina, M.; Jindřich, J.; Šaman, D.; Trnka, T. Improved Synthesis of 1,2-trans-Acetates and 1,2-trans Ethyl 1-Thioglycosides Derived from 3,4,6-Tri-O-acetyl-2-deoxy-2-phthalimido-D-hexopyranosides. Collection of Czechoslovak Chemical Communications 2003, 68 (7), 1264-1274 DOI: 10.1135/cccc20031264.
Machara, A.; Werner, L.; Endoma-Arias, M. Ann; D. Cox, P.; Hudlicky, T. Improved Synthesis of Buprenorphine from Thebaine and/or Oripavine via Palladium-Catalyzed N-Demethylation/Acylation and/or Concomitant O-Demethylation. Advanced Synthesis & Catalysis 2012, 354 (4), 613-626 DOI: 10.1002/adsc.201100807.
Tarallo, V.; Kasireddy, S.; Misek, J. In vitro evolution of sulfoxide reductases. Journal of Biotechnology 2019, 305, S30-S30 DOI: 10.1016/j.jbiotec.2019.05.113.
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, 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.
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.
Güixens-Gallardo, P.; Hocek, M.; Perlíková, P. Inhibition of non-templated nucleotide addition by DNA polymerases in primer extension using twisted intercalating nucleic acid modified templates. Bioorganic & Medicinal Chemistry Letters 2016, 26 (2), 288-291 DOI: 10.1016/j.bmcl.2015.12.034.
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