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H
Beier, P.; Chvojka, T.; Janecký, L.; Klepetářová, B.; Markos, A.; Martínek, T.; Martinez-Seara, H. Haloalkenyl Imidoyl Halides as Multifacial Substrates in the Stereoselective Synthesis of N-Alkenyl Compounds. Advanced Synthesis and Catalysis 2021, 363 (13), 3258-3266.
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.
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.
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.
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.
I
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.
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.
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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