Vyhledat publikace
Liška, A.; Chrenko, D.; Zatloukalová, M.; Klíma, J.; Papoušková, B.; Kabeláč, M.; Ludvík, J.; Pospíšil, J.; Vacek, J.
Redox Behaviour of Nitro-Fatty Acids and Their Ester
Electrochimica Acta 2026, 545 (n/a), 147698 (p. 1-12). DOI: 10.1016/j.electacta.2025.147698
Orság, Š.; Frydrych, I.; Lišková, B.; Gurská, S.; Přibylka, A.; Hodoň, J.; Džubák, P.; Hajdúch, M. Urban, M.
Synthesis and biological evaluation of novel C-30 modified lupane triterpenoids selectively cytotoxic against cancer cells
Eur. J. Med. Chem. 2026, 302 ((-)), 118268. DOI: 10.1016/j.ejmech.2025.118268
Chasák, J.; Vyvlečka, P.; Nemec, I.; Matheeussen, A.; Van Pelt, N.; Cos, P.; Caljon, G.; Kryštof, V.; Brulíková, L.*
Cytotoxicity and Antimicrobial Activity Of GaMF1 Analogues
Chem. Med. Chem. 2026, 21 (4), e202500951 (1-17). DOI: 10.1002/cmdc.202500951
Stehlík, J., Pocklanová, R., Profous, D., Lapčíková, B., Cankař, P., Kvítek, L., Lapčík, Ľ
Innovative Copper-Based Heterogeneous Catalyst for Chan–Lam Cross-Coupling
Catalysts 2026, 16 (I), 94(1-14). DOI: https://doi.org/10.3390/catal16010094
Profous, D.; Cankařová, N.; Enengl, J.; Soji, S.; Rinner, U.; Jurečka, P.; Cankař, P.
Second-Generation Synthesis and Analytical Application of TBBA for Chiral Analysis of Amino Acids and Oligopeptides by 1H and 19F NMR Spectroscopy
J. Org. Chem. 2026, 91 (5), 2065-2073. DOI: 10.1021/acs.joc.5c02693
Valenta, M.; Stýskala, J.
Chemical Modification of 2,6,9-Trisubstituted Purine CDK Inhibitors: tert-Butylation at N7/N9 and Access to 2,6,7-Trisubstituted Analogs
ACS Omega 2026, 11 (16), 23833-23844. DOI: 10.1021/acsomega.5c10284
Bachořík, J.; Frydrych, I.; Gurská, S.; Dostál, Š.; Pokorný, J.; Džubák, P.; Hajdúch, M.; Urban, M.
New Synthetic Approach to C‑30 Ethers, Esters, and Amines of Betulin Using the Mitsunobu Reaction and Biological Evaluation of the Products
ACS Omega 2026, 11 (16), 24564-24579. DOI: 10.1021/acsomega.6c00716
Kristek, J.; Šťastná, N.; Pospíšil, J.
Base-Promoted C→N Carbonyl Shift Enables One-Step Access to aza-β-Lactams from α‑Heteroaryl-α-amino Esters
Org. Lett. 2026, 28 (20), 6318-6323. DOI: 10.1021/acs.orglett.6c01451
Toman, D.; Nemec, I.; Kurka, O.; Přibylka, A.; Cankař, P.
Axially chiral dimethylaminobenzimidazoles and their preliminary evaluation as acyl-transfer reagents
Org. Biomol. Chem. 2025, 23 (11), 2672-2682. DOI: 10.1039/D4OB02052A
Zůvalová, I.; Vyhlídalová, B.; Ondrová, K..; Nádvorník, P.; Hrubý, J.; Illés, P.; Soural, M.; Šebela, M.; Šindlerová, L.; Kubala, L.; Mani, S.; Dvořák, Z.
Decoding structural determinants of aryl hydrocarbon receptor antagonism by monoterpenoids
Bioorg. Chem. 2025, – (-), 108265. DOI: doi.org/10.1016/j.bioorg.2025.108265