| Synthesis of S-Linked Glycoconjugates and S-Disaccharides by Thiol–Ene Coupling Reaction of Enoses L Lázár, M Csávás, M Herczeg, P Herczegh, A Borbás Organic letters 14 (17), 4650-4653, 2012 | 95 | 2012 |
| Systematic study on free radical hydrothiolation of unsaturated monosaccharide derivatives with exo-and endocyclic double bonds L Lázár, M Csávás, Á Hadházi, M Herczeg, M Tóth, L Somsák, T Barna, ... Organic & Biomolecular Chemistry 11 (32), 5339-5350, 2013 | 55 | 2013 |
| Synthesis and anticoagulant activity of bioisosteric sulfonic‐acid analogues of the antithrombin‐binding pentasaccharide domain of heparin M Herczeg, L Lázár, Z Bereczky, KE Kövér, I Timári, J Kappelmayer, ... Chemistry–A European Journal 18 (34), 10643-10652, 2012 | 37 | 2012 |
| Toward synthesis of the isosteric sulfonate analogues of the AT-III binding domain of heparin M Herczeg, L Lázár, A Borbás, A Lipták, S Antus Organic Letters 11 (12), 2619-2622, 2009 | 31 | 2009 |
| Synthesis of the non-reducing end trisaccharide of the antithrombin-binding domain of heparin and its bioisosteric sulfonic acid analogues L Lázár, E Mező, M Herczeg, A Lipták, S Antus, A Borbás Tetrahedron 68 (36), 7386-7399, 2012 | 30 | 2012 |
| A low-temperature, photoinduced thiol–ene click reaction: a mild and efficient method for the synthesis of sugar-modified nucleosides M Bege, I Bereczki, M Herczeg, M Kicsák, D Eszenyi, P Herczegh, ... Organic & Biomolecular Chemistry 15 (43), 9226-9233, 2017 | 28 | 2017 |
| Tricyclanos: conformationally constrained nucleoside analogues with a new heterotricycle obtained from ad-ribofuranose unit M Kicsák, A Mándi, S Varga, M Herczeg, G Batta, A Bényei, A Borbás, ... Organic & Biomolecular Chemistry 16 (3), 393-401, 2018 | 26 | 2018 |
| Synthesis of disaccharide fragments of the AT-III binding domain of heparin and their sulfonatomethyl analogues M Herczeg, L Lázár, A Mándi, A Borbás, I Komáromi, A Lipták, S Antus Carbohydrate research 346 (13), 1827-1836, 2011 | 24 | 2011 |
| Comparison of carbohydrate force fields using Gaussian Accelerated Molecular Dynamics simulations and development of force field parameters for heparin-analogue pentasaccharides G Balogh, T Gyongyosi, I Timári, M Herczeg, A Borbás, K Fehér, KE Kover Journal of Chemical Information and Modeling 59 (11), 4855-4867, 2019 | 22 | 2019 |
| A three-component reagent system for rapid and mild removal of O-, N-and S-trityl protecting groups M Kicsák, M Bege, I Bereczki, M Csávás, M Herczeg, Z Kupihár, L Kovács, ... Organic & Biomolecular Chemistry 14 (12), 3190-3192, 2016 | 22 | 2016 |
| Synthesis and antibacterial evaluation of some teicoplanin pseudoaglycon derivatives containing alkyl-and arylthiosubstituted maleimides M Csávás, A Miskovics, Z Szűcs, E Rőth, ZL Nagy, I Bereczki, M Herczeg, ... The Journal of Antibiotics 68 (9), 579-585, 2015 | 22 | 2015 |
| Novel syntheses of Idraparinux, the anticoagulant pentasaccharide with indirect selective factor Xa inhibitory activity M Herczeg, E Mező, L Lázár, A Fekete, KE Kövér, S Antus, A Borbás Tetrahedron 69 (15), 3149-3158, 2013 | 22 | 2013 |
| New synthesis of idraparinux, the non-glycosaminoglycan analogue of the antithrombin-binding domain of heparin M Herczeg, E Mező, D Eszenyi, S Antus, A Borbás Tetrahedron 70 (18), 2919-2927, 2014 | 19 | 2014 |
| Synthesis of sulfonic acid analogues of the non-reducing end trisaccharide of the antithrombin binding domain of heparin L Lázár, M Herczeg, A Fekete, A Borbás, A Lipták, S Antus Tetrahedron Letters 51 (51), 6711-6714, 2010 | 19 | 2010 |
| Rhamnose Binding Protein as an Anti-Bacterial Agent—Targeting Biofilm of Pseudomonas aeruginosa TK Fu, SK Ng, YE Chen, YC Lee, F Demeter, M Herczeg, A Borbás, ... Marine drugs 17 (6), 355, 2019 | 17 | 2019 |
| Rapid synthesis of self-assembling 1, 2-thiomannobioside glycoconjugates as potential multivalent ligands of mannose-binding lectins M Csávás, T Demeter, M Herczeg, I Timári, KE Kövér, P Herczegh, ... Tetrahedron letters 55 (51), 6983-6986, 2014 | 17 | 2014 |
| Large-scale synthesis of 6-deoxy-6-sulfonatomethyl glycosides and their application for novel synthesis of a heparinoid pentasaccharide trisulfonic acid of anticoagulant activity E Mező, M Herczeg, D Eszenyi, A Borbás Carbohydrate research 388, 19-29, 2014 | 17 | 2014 |
| Inhibitory Effect of Multivalent Rhamnobiosides on Recombinant Horseshoe Crab Plasma Lectin Interactions with Pseudomonas aeruginosa PAO1 M Herczeg, E Mező, N Molnar, SK Ng, YC Lee, M Dah‐Tsyr Chang, ... Chemistry–An Asian Journal 11 (23), 3398-3413, 2016 | 16 | 2016 |
| Synthesis of α‐l‐Fucopyranoside‐Presenting Glycoclusters and Investigation of Their Interaction with Photorhabdus asymbiotica Lectin (PHL) G Jančaříková, M Herczeg, E Fujdiarová, J Houser, KE Kövér, A Borbás, ... Chemistry–A European Journal 24 (16), 4055-4068, 2018 | 13 | 2018 |
| Synthesis of β-d-galactopyranoside-Presenting Glycoclusters, Investigation of Their Interactions with Pseudomonas aeruginosa Lectin A (PA-IL) and Evaluation of … L Malinovská, ST Le, M Herczeg, M Vašková, J Houser, E Fujdiarová, ... Biomolecules 9 (11), 686, 2019 | 12 | 2019 |
Magdolna CsávásMolecular Recognition and Interaction Research Group, University of DebrecenVerified email at science.unideb.hu
