Publikace

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Vyhledat publikace

Šamšulová, V.; Poláková, M.; Horák, R.; Šedivá, M.; Kvapil, L.; Hradil, P.
Synthetic approach to novel glycosyltriazole-3-hydroxyquinolone conjugates and their antimicrobial properties
J. Mol. Struct. 2019, 1177 (-), 16-25. DOI: https://doi.org/10.1016/j.molstruc.2018.09.030

Vanda, D.; Soural, M.; Canale, V.; Chaumont-Dubel, S.; Satała, G.; Kos, T.; Funk, P.; Fülöpová, V.; Lemrová, B.; Koczurkiewicz, P.; Pękala, E.; Bojarski, A.J.; Popik, P.; Marin, P.; Zajdel, P.
Novel non-sulfonamide 5-HT6 receptor partial inverse agonist in a group of imidazo[4,5-b]pyridines with cognition enhancing properties
Eur. J. Med. Chem. 2018, 144 (-), 716-729. DOI: 10.1016/j.ejmech.2017.12.053

Ručilová, V.; Maloň, M.; Soural, M.
Use of Triethylsilane for Directed Enantioselective Reduction of Olefines: Synthesis of Pyrazino[2,1-c][1,4]oxazine-6,9-diones with Full Control of the Absolute Configuration
Eur. J. Org. Chem. 2018, 2018 (4), 564-570. DOI: 10.1002/ejoc.201701553

Konrádová, D.; Bon, D. J.-Y. D.; Pospíšil, J.
1-(Phenylsulfonyl)-3-oxabicyclo[3.1.0]hexan-2-one as a building block in organic synthesis
J. Org. Chem. 2018, 83 (12229), 12229-12238. DOI: 10.1021/acs.joc.8b01625

Horák, R.; Kvapil, L.; Motyka, K.; Slaninová, L.; Grepl, M.; Kořistek, K.; Urbášek, M.; Hradil, P; Soural, M.
Synthesis of 2-alkenyl-3-hydroxyquinolin-4(1H)-ones as promising antimicrobial and fluorescent agents
Tetrahedron 2018, 74 (2), 366-374. DOI: 10.1016/j.tet.2017.12.010

Trapani, P.; Kvapil, L.; Hradil, P.; Soural, M.
Use of Phenacylthiosalicylates for the Preparation of 3-Hydroxybenzo[b]thiophene Derivatives
Synlett 2018, 29 (6), 810-814. DOI: 10.1055/s-0036-1591875

Pokorný, J.; Borková, L.; Urban, M.
Click Reactions in Chemistry of Triterpenes – Advances Towards Development of Potential Therapeutics
Current Med. Chem. 2018, 25 (5), 636-658. DOI: 10.2174/0929867324666171009122612

Béres, T.; Dragull, K.; Pospíšil, J.; Tarkowská, D.; Dančák, M.; Bíba, O.; Tarkowski, P.; Doležal, K.; Strnad, M.
Quantitative Analysis of Ingenol in Euphorbia species via Validated Isotope Dilution Ultra-high Performance Liquid Chromatography Tandem Mass Spectrometry
Phytochem. Anal. 2018, 29 (1), 23-29. DOI: 10.1002/pca.2711

Barbuščáková, Z.; Kozubíková, H.; Zálešák, F.; Doležal, K.; Pospíšil, J.
General approach to neoliganane-core of the boehmenan natural product family
Monatsh. Chem. 2018, 149 (4), 737-748. DOI: 10.1007/s00706-017-2132-4

Pokorný, J.; Krajčovičová, S.; Hajdúch, M.; Holoubek, M.; Gurská, S.; Džubák, P.; Volná, T.; Popa, I.; Urban, M.
Triterpenic azines, a new class of compounds with selective cytotoxicity to leukemia cells CCRF-CEM
Future Med. Chem. 2018, 10 (5), 483-491. DOI: https://doi.org/10.4155/fmc-2017-0171