Publications

Novák, P.; Pohl, R.; Kotora, M.; Hocek, M. Synthesis of C-Aryldeoxyribosides by [2 + 2 + 2]-Cyclotrimerization Catalyzed by Rh, Ni, Co, and Ru Complexes. Organic Letters 2006, 8 (10), 2051-2054 DOI: 10.1021/ol060454m.

Nosek, V.; Míšek, J. Sulfinamide Crossover Reaction. Journal of Organic Chemistry 2024, 89 (11), 7927-7932.

Nosek, V.; Míšek, J. Chemoenzymatic Deracemization of Chiral Sulfoxides. Angewandte Chemie-International Edition 2018, 57 (31), 9849-9852 DOI: 10.1002/anie.201805858.

Nomura, K.; Mancuso, R.; Cai, Z.; Dagorne, S.; Eisen, M. S.; Gonsalvi, L.; Kotora, M.; Lee, B. Yeoul; Liu, S.; Martins, L. Margarida; et al. Exclusive Papers of the Editorial Board Members and Topical Advisory Panel Members of Catalysts in Section "Catalysis in Organic and Polymer Chemistry". Catalysts 2024, 14 (7).

Nigríni, M.; Bhosale, V. Anandrao; Císařová, I.; Veselý, J. Enantioenriched 1,4-Benzoxazepines via Chiral Brønsted Acid-Catalyzed Enantioselective Desymmetrization of 3-Substituted Oxetanes. Journal of Organic Chemistry 2023, 88 (24), 17024-17036.

Nečas, D.; Hidasová, D.; Hocek, M.; Kotora, M. Modular synthesis of 1-α- and 1-β-(indol-2-yl)-2′-deoxyribose C-nucleosides. Organic & Biomolecular Chemistry 2011, 9 (17), 5934 DOI: 10.1039/c1ob05844d.

Nečas, D.; Ramella, D.; Rudovská, I.; Kotora, M. Ni(ethylhexanoate)2/nligand/Et2AlCl catalyzed cycloisomerization of 1,6-heptadienes to cyclopentane derivatives. Journal of Molecular Catalysis A: Chemical 2007, 274 (1-2), 78-82 DOI: 10.1016/j.molcata.2007.04.032.

Nečas, D.; Kotora, M. Rhodium-Catalyzed C-C Bond Cleavage Reactions. Current Organic Chemistry 2007, 11 (17), 1566-1591 DOI: 10.2174/138527207782418645.

Nečas, D.; Drabina, P.; Sedlák, M.; Kotora, M. Fe-Catalyzed reactions of 2-chloro-1,7-dienes and allylmalonates. Tetrahedron Letters 2007, 48 (26), 4539-4541 DOI: 10.1016/j.tetlet.2007.04.143.

Nečas, D.; Kotora, M. Ring Opening of Methylenecycloalkenes via the C−C Bond Cleavage. Organic Letters 2008, 10 (22), 5261-5263 DOI: 10.1021/ol801728f.

Navrátilová, K.; Řezanka, P.; Řezanka, M.; Sýkora, D.; Jindřich, J.; Král, V. The study of enantioselectivity of all regioisomers of mono-carboxymethyl-β-cyclodextrin used as chiral selectors in CE. Journal of Separation Science 2013, 36 (7), 1270–1274 DOI: 10.1002/jssc.201201144.

Navrátil, R.; Kellovská, K.; Baszczyňski, O. Multimetallic Pd- and Ni-catalyzed C(sp²)–P cross-coupling under aqueous micellar conditions. Green Chemistry 2023, 25 (23), 9779-9794.

Nauš, P.; Caletková, O.; Konečný, P.; Džubák, P.; Bogdanová, K.; Kolář, M.; Vrbková, J.; Slavětínská, L.; Tloušt’ová, E.; Perlíková, P.; et al. Synthesis, Cytostatic, Antimicrobial, and Anti-HCV Activity of 6-Substituted 7-(Het)aryl-7-deazapurine Ribonucleosides. Journal of Medicinal Chemistry 2014, 57 (3), 1097-1110 DOI: 10.1021/jm4018948.

Nauš, P.; Perlíková, P.; Bourderioux, A.; Pohl, R.; Slavětínská, L.; Votruba, I.; Bahador, G.; Birkuš, G.; Cihlář, T.; Hocek, M. Sugar-modified derivatives of cytostatic 7-(het)aryl-7-deazaadenosines: 2′-C-methylribonucleosides, 2′-deoxy-2′-fluoroarabinonucleosides, arabinonucleosides and 2′-deoxyribonucleosides. Bioorganic & Medicinal Chemistry 2012, 20 (17), 5202-5214 DOI: 10.1016/j.bmc.2012.07.003.

Nauš, P.; Caletková, O.; Perlíková, P.; Slavětínská, L. Poštová; Tloušťová, E.; Hodek, J.; Weber, J.; Džubák, P.; Hajdúch, M.; Hocek, M. Synthesis and biological profiling of 6- or 7-(het)aryl-7-deazapurine 4′-C-methylribonucleosides. Bioorganic & Medicinal Chemistry 2015, 23 (23), 7422-7438 DOI: 10.1016/j.bmc.2015.10.040.

Nallappan, S.; Lapinskaite, R.; Hájíček, J.; Kunák, D.; Čambal, P.; Nečas, D.; Císařová, I.; Atalay, H. Nazlican; Tumer, T. Boyunegmez; Tarábek, J.; et al. The Biomimetic Synthesis of Polyarylated Fluorenes, Relevant to Selaginellaceae Polyphenols, Leading to the Spontaneous Formation of Stable Radicals. ChemPlusChem 2024, 89 (4).

Nallappan, S.; Kucherak, O.; Kiss, A.; Lapinskaite, R.; Císařová, I.; Rýček, L. Internal 2D networking of silver bromide with a bidentate N-heterocyclic carbene ligand enables the formation of an inherently heterogeneous reusable catalyst for multicomponent A³ coupling. New Journal of Chemistry 2024, 48 (28), 12800-12806.

Nakatani, K.; Tor, Y.; Dadová, J.; Cahová, H.; Hocek, M. Polymerase Synthesis of Base-Modified DNA; Springer International Publishing: Cham, 2016; Vol. 31, pp 123-144.

Nakanishi, T.; Weber, J.; Bojdys, M. J.; Thomas, A. Polymeric Frameworks: Toward Porous Semiconductors; John Wiley & Sons, Inc.: Hoboken, NJ, USA, 2011; pp 119-154.

Murphy, B.; Šnajdr, I.; Machara, A.; Endoma-Arias, M. Ann A.; Stamatatos, T. C.; D. Cox, P.; Hudlicky, T. Conversion of Thebaine to Oripavine and Other Useful Intermediates for the Semisynthesis of Opiate-Derived Agents: Synthesis of Hydromorphone. Advanced Synthesis & Catalysis 2014, 356 (11-12), 2679-2687 DOI: 10.1002/adsc.201400445.

Mulholland, C.; Jestřábová, I.; Sett, A.; Ondruš, M.; Sýkorová, V.; C. Manzanares, L.; Šimončík, O.; Muller, P.; Hocek, M. The selection of a hydrophobic 7-phenylbutyl-7-deazaadenine-modified DNA aptamer with high binding affinity for the Heat Shock Protein 70. Communications Chemistry 2023, 6 (1).

Motloch, P.; Blahut, J.; Císařová, I.; Roithová, J. X-ray characterization of triphenylphosphine-gold(I) olefin pi-complexes and the revision of their stability in solution. Journal of Organometallic Chemistry 2017, 848, 114-117 DOI: 10.1016/j.jorganchem.2017.07.011.

Motloch, P.; Valterová, I.; Kotora, M. Enantioselective Allylation of Thiophene-2-carbaldehyde: Formal Total Synthesis of Duloxetine. Advanced Synthesis & Catalysis 2014, 356 (1), 199-204 DOI: 10.1002/adsc.201300849.

Misehe, M.; Šála, M.; Matoušová, M.; Hercík, K.; Kocek, H.; Chalupská, D.; Chaloupecká, E.; Hájek, M.; Bouřa, E.; Mertlíková-Kaiserová, H.; et al. Design, synthesis and evaluation of novel thieno[2,3d]pyrimidine derivatives as potent and specific RIPK2 inhibitors. Bioorganic and Medicinal Chemistry Letters 2024, 97 (1 January 2024).

Misehe, M.; Matoušová, M.; Dvořáková, A.; Hercík, K.; Škach, K.; Chalupská, D.; Dejmek, M.; Šála, M.; Hájek, M.; Bouřa, E.; et al. Exploring positions 6 and 7 of a quinazoline-based scaffold leads to changes in selectivity and potency towards RIPK2/3 kinases. European Journal of Medicinal Chemistry 2023, 260 (November).