Search Results - "Molnár, Barnabás"

Stereoselective Synthesis and Catalytical Application of Perillaldehyde-Based 3-Amino-1,2-diol Regioisomers by Háznagy, Márton Benedek, Csámpai, Antal, Ugrai, Imre, Molnár, Barnabás, Haukka, Matti, Szakonyi, Zsolt

“…A library of regioisomeric monoterpene-based aminodiols was synthesised and applied as chiral catalysts in the addition of diethylzinc to benzaldehyde. The…”
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Multistep Synthesis and In Vitro Anticancer Evaluation of 2-Pyrazolyl-Estradiol Derivatives, Pyrazolocoumarin-Estradiol Hybrids and Analogous Compounds by Molnár, Barnabás, Gopisetty, Mohana Krishna, Adamecz, Dóra Izabella, Kiricsi, Mónika, Frank, Éva

“…Although the hormone independent cytotoxic activity of several estradiol derivatives endowed with a simple substituent at C-2 has been reported so far,…”
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Microwave-Assisted Stereoselective Heterocyclization to Novel Ring d-fused Arylpyrazolines in the Estrone Series by Mótyán, Gergő, Molnár, Barnabás, Wölfling, János, Frank, Éva

“…Microwave-assisted syntheses of novel ring d-condensed 2-pyrazolines in the estrone series were efficiently carried out from steroidal ,-enones and hydrazine…”
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Efficient access to domain-integrated estradiol-flavone hybrids via the corresponding chalcones and their in vitro anticancer potential by Molnár, Barnabás, Gopisetty, Mohana K., Nagy, Ferenc István, Adamecz, Dóra Izabella, Kása, Zsolt, Kiricsi, Mónika, Frank, Éva

“…[Display omitted] •Novel estradiol-chalcone and estradiol-flavone hybrids were synthesized.•Framework integration was achieved via molecular…”
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Regioselective synthesis, physicochemical properties and anticancer activity of 2-aminomethylated estrone derivatives by Molnár, Barnabás, Kinyua, Njangiru Isaac, Mótyán, Gergő, Leits, Péter, Zupkó, István, Minorics, Renáta, Balogh, György T., Frank, Éva

“…[Display omitted] •Regioselective A-ring-aminomethylation of estrone was developed.•aza-Michael addition of secondary amines to an o-QM intermediate was…”
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Comparative Solution Equilibrium Studies on Anticancer Estradiol-Based Conjugates and Their Copper Complexes by Enyedy, Éva A, Giricz, Anett, Petrasheuskaya, Tatsiana V, Mészáros, János P, May, Nóra V, Spengler, Gabriella, Kovács, Ferenc, Molnár, Barnabás, Frank, Éva

“…Steroids are often considered valuable molecular tools for the development of anticancer agents with improved pharmacological properties. Conjugation of metal…”
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Treating logical fallacies in a normative computational framework of perceptual decision making by Molnár, Barnabás, Koblinger, Ádám, Fiser, József

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Synthesis of novel 17-triazolyl-androst-5-en-3-ol epimers via Cu(I)-catalyzed azide-alkyne cycloaddition and their inhibitory effect on 17α-hydroxylase/C17,20-lyase by Kiss, Anita, Herman, Bianka Edina, Görbe, Tamás, Mernyák, Erzsébet, Molnár, Barnabás, Wölfling, János, Szécsi, Mihály, Schneider, Gyula

“…[Display omitted] •Synthesis of 1′,4′-substituted-1,2,3-triazolyl epimeric androstane derivatives.•The in vitro inhibitory effect of the triazoles on…”
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Synthesis of novel 17-triazolyl-androst-5-en-3-ol epimers via Cu(I)-catalyzed azide-alkyne cycloaddition and their inhibitory effect on 17α-hydroxylase/C 17,20 -lyase by Kiss, Anita, Herman, Bianka Edina, Görbe, Tamás, Mernyák, Erzsébet, Molnár, Barnabás, Wölfling, János, Szécsi, Mihály, Schneider, Gyula

“…The regioselective Cu(I)-catalyzed 1,3-dipolar cycloaddition of 17α- and 17β-azidoandrost-5-en-3β-ol epimers (3b and 5b) with different terminal alkynes…”
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Ösztránvázas Aza- És Oxaciklusos Vegyületek Régiószelektív Szintézise by Barnabás, Molnár

“…A doktori munkám során a kitűzött célokat sikeresen megvalósítottam, az ösztránváz A-gyűrűjének szelektív módosításai révén kapcsolt vagy kondenzált…”
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Synthesis of novel 17-triazolyl-androst-5-en-3-ol epimers via Cu(I)-catalyzed azide-alkyne cycloaddition and their inhibitory effect on 17 alpha-hydroxylase/ C-17,C-20-lyase by Kiss, Anita, Herman, Bianka Edina, Görbe, Tamás, Mernyak, Erzsebet, Molnar, Barnabas, Wolfling, Janos, Szecsi, Mihaly, Schneider, Gyula

“…The regioselective Cu(I)-catalyzed 1,3-dipolar cycloaddition of 17 alpha- and 17 beta-azidoandrost-5-en-3 beta-ol epimers (3b and 5b) with different terminal…”
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