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Autorské časopisecké publikace

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Tomanová, M.; Kozlanská, K.; Jorda, R.; Jedinák, L.; Havlíková, T.; Řezníčková, E.; Peřina, M.; Klener, P.; Dolníková, A.; Cankař, P.; Kryštof, V.
Synthesis and Structural Optimization of 2,7,9-Trisubstituted purin-8-ones as FLT3-ITD Inhibitors
Int. J. Mol. Sci. 2022, 23 (24), 16169. DOI: 10.3390/ijms232416169

Hernychová, L.; Alexandri, E.; Tzakos, A. G.; Zatloukalová, M.; Primikyri, A.; Gerothanassis, I. P.; Uhrik, L.; Šebela, M.; Kopečný, D.; Jedinák, L.; Vacek, J.
Serum albumin as a primary non-covalent binding protein for nitro-oleic acid
Int. J. Biol. Macromol. 2022, 2022 (203) (4), 116-129. DOI: 10.1016/j.ijbiomac.2022.01.050

Sobczak, K.; Rudnicki, K.; Jedinak, L.; Zatloukalova, M.; Vacek, J.; Poltorak, L.
Oleic and nitro-oleic acid behavior at an electrified water-1,2-dichloroethane interface
J. Mol. Liquids 2022, 2022 (365) (N/A), 120110(1-6). DOI: 10.1016/j.molliq.2022.120110

Zatloukalová, M.; Jedinák, L.; Riman, D.; Franková, D.; Novák, D.; Cytryniak, A.; Nazaruk, E.; Bilewicz, R.; Vrba, J.; Papoušková, B.; Kabeláč, M.; Vacek, J.
Cubosomal lipid formulation of nitroalkene fatty acids: Preparation, stability and biological effects
Redox Biology 2021, 46 (n/a), 102097(1-14). DOI: 10.1016/j.redox.2021.102097

Tomanová, M.; Jedinák, L.; Cankař, P.
Reductive dehalogenation and dehalogenative sulfonation of phenols and heteroaromatics with sodium sulfite in an aqueous medium
Green Chem. 2019, 21 (10), 2621-2628. DOI: 10.1039/c9gc00467j

Janíková, K.; Jedinák, L.; Volná, T.; Cankař, P.
Chan-​Lam cross-​coupling reaction based on the Cu2S​/TMEDA system
Tetrahedron 2018, 74 (5), 606-617. DOI: 10.1016/j.tet.2017.12.042

Jedinák, L.; Zátopková, R.; Zemánková, H.; Šustková, A.; Cankař, P.
The Suzuki–Miyaura Cross-Coupling Reaction of Halogenated Aminopyrazoles: Method Development, Scope, and Mechanism of Dehalogenation Side Reaction
J. Org. Chem. 2017, 82 (1), 157-169. DOI: 10.1021/acs.joc.6b02306

Tomanová, M.; Jedinák, L.; Košař, J.; Kvapil, L.; Hradil, P.; Cankař, P.
Synthesis of 4-substituted pyrazole-3,5-diamines via Suzuki–Miyaura coupling and iron-catalyzed reduction
Org. Biomol. Chem. 2017, 15 (48), 10200–10211. DOI: 10.1039/c7ob02373a

Jedinák, L.; Kryštof, V.; Cankař, P.
The Synthesis and Biological Evaluation of N-Substituted 1H-Benzimidazol-2-yl-1H-pyrazole-3,5-diamines
J. Heterocycl. Chem. 2016, 53 (2), 499-507. DOI: 10.1002/jhet.2315

Jedinák, L.; Cankař, P.
4-Arylation of N-Acylamino- and Aminopyrazoles by the Suzuki–Miyaura Cross-Coupling Reaction
Eur. J. Org. Chem. 2016, 2016 (11), 2013-2023. DOI: 10.1002/ejoc.201600072