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Mihály Herczeg

Observed names: HERCZEG Mihály, Herczeg, M., Herczeg, Mihály, Herczeg, Mihály, M Herczeg, M. Herczeg, Mihaly Herczeg
ORCID: 0000-0002-7938-9789
Observed ORCID: 0000-0002-7938-9789
OpenAlex ID: A5070386391
Synthesis of S-Linked Glycoconjugates and S-Disaccharides by Thiol–Ene Coupling Reaction of Enoses
2012 · László Lázár, Magdolna Csávás, et al. · Organic Letters · 86
Systematic study on free radical hydrothiolation of unsaturated monosaccharide derivatives with exo- and endocyclic double bonds
2013 · László Lázár, Magdolna Csávás, et al. · Organic & Biomolecular Chemistry · 49
A low-temperature, photoinduced thiol–ene click reaction: a mild and efficient method for the synthesis of sugar-modified nucleosides
2017 · Miklós Bege, Ilona Bereczki, et al. · Organic & Biomolecular Chemistry · 33
Synthesis and Anticoagulant Activity of Bioisosteric Sulfonic‐Acid Analogues of the Antithrombin‐Binding Pentasaccharide Domain of Heparin
2012 · Mihály Herczeg, László Lázár, et al. · Chemistry - A European Journal · 33
Tricyclanos: conformationally constrained nucleoside analogues with a new heterotricycle obtained from a d -ribofuranose unit
2017 · Máté Kicsák, Attila Mándi, et al. · Organic & Biomolecular Chemistry · 28
A three-component reagent system for rapid and mild removal of O-, N- and S-trityl protecting groups
2016 · Máté Kicsák, Miklós Bege, et al. · Organic & Biomolecular Chemistry · 28
Synthesis of the non-reducing end trisaccharide of the antithrombin-binding domain of heparin and its bioisosteric sulfonic acid analogues
2012 · László Lázár, Erika Mező, et al. · Tetrahedron · 26
Comparison of Carbohydrate Force Fields Using Gaussian Accelerated Molecular Dynamics Simulations and Development of Force Field Parameters for Heparin-Analogue Pentasaccharides
2019 · Gábor Balogh, Tamás Gyöngyösi, et al. · Journal of Chemical Information and Modeling · 25
Toward Synthesis of the Isosteric Sulfonate Analogues of the AT-III Binding Domain of Heparin
2009 · Mihály Herczeg, László Lázár, et al. · Organic Letters · 25
Synthesis of disaccharide fragments of the AT-III binding domain of heparin and their sulfonatomethyl analogues
2011 · Mihály Herczeg, László Lázár, et al. · Carbohydrate Research · 24
Synthesis and antibacterial evaluation of some teicoplanin pseudoaglycon derivatives containing alkyl- and arylthiosubstituted maleimides
2015 · Dedicated to the memory of Professor Maria N Preobrazhenskaya, Magdolna Csávás, et al. · The Journal of Antibiotics · 23
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Rhamnose Binding Protein as an Anti-Bacterial Agent—Targeting Biofilm of Pseudomonas aeruginosa
2019 · Tse-Kai Fu, Sim-Kun Ng, et al. · Marine Drugs · 20
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Photoinitiated Thiol−Ene Reactions of Various 2,3‐Unsaturated O‐, C‐ S‐ and N‐Glycosides – Scope and Limitations Study
2020 · Viktor Kelemen, Magdolna Csávás, et al. · Chemistry - An Asian Journal · 19
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New synthesis of idraparinux, the non-glycosaminoglycan analogue of the antithrombin-binding domain of heparin
2014 · Mihály Herczeg, Erika Mező, et al. · Tetrahedron · 19
Novel syntheses of Idraparinux, the anticoagulant pentasaccharide with indirect selective factor Xa inhibitory activity
2013 · Mihály Herczeg, Erika Mező, et al. · Tetrahedron · 19
Mannich-type modifications of (−)-cannabidiol and (−)-cannabigerol leading to new, bioactive derivatives
2023 · Eszter Boglárka Lőrincz, Gergely Tóth, et al. · Scientific Reports · 17
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Inhibitory Effect of Multivalent Rhamnobiosides on Recombinant Horseshoe Crab Plasma Lectin Interactions with Pseudomonas aeruginosa PAO1
2016 · Mihály Herczeg, Erika Mező, et al. · Chemistry - An Asian Journal · 16
Large-scale synthesis of 6-deoxy-6-sulfonatomethyl glycosides and their application for novel synthesis of a heparinoid pentasaccharide trisulfonic acid of anticoagulant activity
2014 · Erika Mező, Mihály Herczeg, et al. · Carbohydrate Research · 16
Replacement of the L-iduronic acid unit of the anticoagulant pentasaccharide idraparinux by a 6-deoxy-L-talopyranose – Synthesis and conformational analysis
2018 · Fruzsina Demeter, Tamás Gyöngyösi, et al. · Scientific Reports · 15
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Rapid synthesis of self-assembling 1,2-thiomannobioside glycoconjugates as potential multivalent ligands of mannose-binding lectins
2014 · Magdolna Csávás, Tamás Demeter, et al. · Tetrahedron Letters · 15
Synthesis of sulfonic acid analogues of the non-reducing end trisaccharide of the antithrombin binding domain of heparin
2010 · László Lázár, Mihály Herczeg, et al. · Tetrahedron Letters · 15
Tightly linked morpholino-nucleoside chimeras: new, compact cationic oligonucleotide analogues
2021 · Nóra Debreczeni, Miklós Bege, et al. · Organic & Biomolecular Chemistry · 14
Synthesis of 6‐Sulfonatomethyl Thioglycosides by Nucleophilic Substitution: Methods to Prevent 1→6 Anomeric Group Migration of Thioglycoside 6‐O‐Triflates
2013 · Mihály Herczeg, Erika Mező, et al. · European Journal of Organic Chemistry · 14
Synthesis of β-d-galactopyranoside-Presenting Glycoclusters, Investigation of Their Interactions with Pseudomonas aeruginosa Lectin A (PA-IL) and Evaluation of Their Anti-Adhesion Potential
2019 · Lenka Malinovská, Son Thai Le, et al. · Biomolecules · 13
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Simultaneous Application of Arylmethylene Acetal and Butane Diacetal Groups for Protection of Hexopyranosides: Synthesis and Chemoselective Ring‐Opening Reactions
2015 · Mihály Herczeg, Fruzsina Demeter, et al. · European Journal of Organic Chemistry · 13
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Works count: 99
Citation count: 804
H-index: 16
I10-index: 31
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