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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
Pokorný, J.; Horka, V.; Šidová, V.; Urban, M.
Synthesis and characterization of new conjugates of betulin diacetate and bis(triphenysilyl) betulin with substituted triazoles
Monatsh. Chem. 2018, 149 (4), 839-845. DOI: 10.1007/s00706-017-2113-7
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Modification of Boc-Protected CAN508 via Acylation and Suzuki-Miyaura Coupling
Molecules 2018, 23 (1), 149-162. DOI: 10.3390/molecules23010149
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
Krajčovičová, S.; Staňková, J.; Džubák, P.; Hajdúch, M.; Soural, M.; Urban, M.
Synthetic approach for rapid preparation of BODIPY conjugates and their use in imaging of cellular drug uptake and distribution
Chem. Eur. J. 2018, 24 (19), 4957-4966. DOI: 10.1002/chem.201706093
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One and two-carbon homologation of primary and secondary alcohols to corresponding carboxylic esters using β-carbonyl BT sulfones as a common intermediate
J. Org. Chem. 2018, 83 (9), 4990-5001. DOI: 10.1021/acs.joc.8b00112
Kralová, P.; Maloň, M.; Koshino, H.; Soural, M.
Convenient synthesis of thiohydantoins, imidazole-2-thiones and imidazo[2,1-b]thiazol-4-iums from polymer-supported alpha-acylamino ketones
Molecules 2018, 23 (4), 976-984. DOI: 10.3390/molecules23040976
Ručilová, V.; Soural, M.
Recent advances in the applications of triethylsilane in organic synthesis
Synthesis 2018, 50 (19), 3809-3824. DOI: 10.1055/s-0037-1610107
Šlachtová, V.; Brulíková, L.*
Benzoxazole Derivatives as Promising Antitubercular Agents
ChemistrySelect 2018, 3 (17), 4653-4662. DOI: 10.1002/slct.201800631