Search Results - "Hergert, Tamás"

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  1. 1

    Click Reactions Meet Flow Chemistry: An Overview of the Applications of Click Chemistry under Continuous Flow Conditions by Kánya, Nándor, Zsigmond, Tamás Sándor, Hergert, Tamás, Lövei, Klára, Dormán, György, Kálmán, Ferenc, Darvas, Ferenc

    Published in Organic process research & development (17-05-2024)
    “…Click reactions are versatile tools in the hands of synthetic chemists and materials scientists around the world. Coupling click chemistry with the advantages…”
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    Journal Article
  2. 2

    Access to Fluorazones by Intramolecular Dehydrative Cyclization of Aromatic Tertiary Amides: A Synthetic and Mechanistic Study by Mátravölgyi, Béla, Hergert, Tamás, Bálint, Erika, Bagi, Péter, Faigl, Ferenc

    Published in Journal of organic chemistry (16-02-2018)
    “…An efficient synthesis has been developed for the preparation of 9H-pyrrolo­[1,2-a]­indol-9-ones (fluorazones) from readily available anthranilic acid…”
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    Journal Article
  3. 3

    Copper-facilitated Suzuki-Miyaura coupling for the preparation of 1,3-dioxolane-protected 5-arylthiophene-2-carboxaldehydes by Hergert, Tamás, Varga, Bálint, Thurner, Angelika, Faigl, Ferenc, Mátravölgyi, Béla

    Published in Tetrahedron (19-04-2018)
    “…5-Formyl-2-thiopheneboronic acid is a widely used building block for the synthesis of diverse structures, however, due to a significant instability its…”
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    Journal Article
  4. 4

    Multistep batch-flow hybrid synthesis of a terbinafine precursor by Hergert, Tamás, Mátravölgyi, Béla, Örkényi, Róbert, Éles, János, Faigl, Ferenc

    Published in Journal of flow chemistry (01-03-2022)
    “…A three-step batch-flow hybrid process has been developed for an expeditious synthesis of the enynol key intermediate of antifungal terbinafine. This procedure…”
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    Journal Article
  5. 5

    Synthesis and Investigation of Solar‐Cell Photosensitizers Having a Fluorazone Backbone by Mátravölgyi, Béla, Hergert, Tamás, Thurner, Angelika, Varga, Bálint, Sangiorgi, Nicola, Bendoni, Riccardo, Zani, Lorenzo, Reginato, Gianna, Calamante, Massimo, Sinicropi, Adalgisa, Sanson, Alessandra, Faigl, Ferenc, Mordini, Alessandro

    Published in European journal of organic chemistry (10-04-2017)
    “…A synthetic sequence for the preparation of fully conjugated 2,7‐disubstituted fluorazone (9H‐pyrrolo[1,2‐‐a]indol‐9‐one) derivatives has been developed…”
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    Journal Article
  6. 6

    Effect of Binding Linkers on the Efficiency and Metabolite Profile of Biomimetic Reactions Catalyzed by Immobilized Metalloporphyrin by Balogh, György T, Decsi, Balázs, Krammer, Réka, Kenéz, Balázs, Ender, Ferenc, Hergert, Tamás, Balogh-Weiser, Diána

    Published in Metabolites (01-12-2022)
    “…The investigation of liver-related metabolic stability of a drug candidate is a widely used key strategy in early-stage drug discovery. Metalloporphyrin-based…”
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    Journal Article
  7. 7

    New P2X3 receptor antagonists. Part 2: Identification and SAR of quinazolinones by Szántó, Gábor, Makó, Attila, Vágó, István, Hergert, Tamás, Bata, Imre, Farkas, Bence, Kolok, Sándor, Vastag, Mónika

    Published in Bioorganic & medicinal chemistry letters (15-08-2016)
    “…[Display omitted] Numerous potent P2X3 antagonists have been discovered and the therapeutic potential of P2X3 antagonism already comprises proof-of-concept…”
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    Journal Article
  8. 8

    A novel and convenient method for the preparation of 5-(diphenylmethylene)-1H-pyrrol-2(5H)-ones; synthesis and mechanistic study by Faigl, Ferenc, Deák, Szilvia, Mucsi, Zoltán, Hergert, Tamás, Balázs, László, Sándor, Boros, Balázs, Barbara, Holczbauer, Tamás, Nyerges, Miklós, Mátravölgyi, Béla

    Published in Tetrahedron (01-09-2016)
    “…An efficient, regioselective synthesis has been developed for the preparation of 5-(diphenylmethylene)-1H-pyrrol-2(5H)-ones from readily available 1H-pyrroles…”
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    Journal Article
  9. 9
  10. 10

    Pirroloindolonok szintézise és felhasználási lehetőségei by Tamás, Hergert

    Published 01-01-2018
    “…Tf2O-vzise és hasznosíthatósági lehetőségeik körében végeztem. Célom egyrészt a vegyületcsalád képviselőinek szintézisére hatékony és általánosan alkalmazható…”
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    Dissertation