Publications

Found 415 results
Author [ Title(Desc)] Type Year
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
F
Herrmann, P.; Buděšínský, M.; Kotora, M. Formal Total Synthesis of (±)-Estrone and Zirconocene-Promoted Cyclization of 2-Fluoro-1,7-octadienes and Ru-Catalyzed Ring Closing Metathesis. The Journal of Organic Chemistry 2008, 73 (16), 6202-6206 DOI: 10.1021/jo800620d.
Jakl, M.; Straka, M.; Dytrtová, J. Jaklová; Roithová, J. Formation and stability of calcium complexes of dimethyl sulfoxide in water. International Journal of Mass Spectrometry 2014, 360, 8-14 DOI: 10.1016/j.ijms.2014.01.001.
Dian, J.; Jindřich, J.; Jelinek, I. Functionalized materials with fluorescent dyes for chemosensor applications. Monatshefte Fur Chemie 2017, 148 (11), 1929-1935 DOI: 10.1007/s00706-017-2041-6.
G
Kopecna, M.; Machacek, M.; Prchalová, E.; Stepanek, P.; Drasar, P.; Kotora, M.; Vavrova, K. Galactosyl Pentadecene Reversibly Enhances Transdermal and Topical Drug Delivery. Pharmaceutical Research 2017, 34 (10), 2097-2108 DOI: 10.1007/s11095-017-2214-3.
Tsybizova, A.; Schröder, D.; Roithová, J.; Henke, A.; Šrogl, J. Gas-phase studies of copper catalyzed aerobic cross coupling of thiol esters and arylboronic acids: REACTION MECHANISMS. Journal of Physical Organic Chemistry 2014, 27 (3), 198-203 DOI: 10.1002/poc.3262.
Kubelka, T.; Slavětínská, L.; Hocek, M. A General Regioselective Approach to 2,4-Disubstituted Pyrimidin-5-yl C-2-Deoxyribonucleosides. Synthesis 2012, 44 (06), 953-965 DOI: 10.1055/s-0031-1289694.
Ćerňová, M.; Pohl, R.; Klepetářová, B.; Hocek, M. A General Regioselective Synthesis of 2,4-Diarylpyrimidines from 2- Thiouracil through Two Orthogonal Cross-Coupling Reactions. Synlett 2012, 23 (09), 1305-1308 DOI: 10.1055/s-0031-1290826.
Caivano, I.; Císařová, I.; Kotora, M.; Nečas, D.; Tošner, Z. A General Synthetic Approach and Photophysical Properties of Regioselectively Fluorinated [5]- and [6]-Helical Bispiroindenofluorenes. ChemPlusChem 2020, 85 (9), 2010-2016 DOI: 10.1002/cplu.202000434.
Baumgartner, B.; Bojdys, M. J.; Unterlass, M. M. Geomimetics for green polymer synthesis: highly ordered polyimides via hydrothermal techniques. Polymer Chemistry 2014, 5 (12), 3771 DOI: 10.1039/c4py00263f.
Riedl, J.; Ménová, P.; Pohl, R.; Orság, P.; Fojta, M.; Hocek, M. GFP-like Fluorophores as DNA Labels for Studying DNA–Protein Interactions. The Journal of Organic Chemistry 2012, 77 (18), 8287-8293 DOI: 10.1021/jo301684b.
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.
Roithová, J.; Gray, A.; Andris, E.; Jašík, J.; Gerlich, D. Helium Tagging Infrared Photodissociation Spectroscopy of Reactive Ions. Accounts of Chemical Research 2016, 49 (2), 223-230 DOI: 10.1021/acs.accounts.5b00489.
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.
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.
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