Márta Palkó

发表

Synthesis of Pyrrolo[1,2-a]pyrimidine Enantiomers via Domino Ring-Closure followed by Retro Diels-Alder Protocol

M. Haukka, F. Fülöp, Beáta Fekete, 2017, Molecules.

A Domino Ring-Closure Followed by Retro-Diels–Alder Reaction for the Preparation of Pyrimido[2,1-a]isoindole Enantiomers

M. Haukka, I. Mándity, F. Fülöp, 2016 .

Synthesis of all four enantiomers of 1-aminoindane-2-carboxylic acid, a new cispentacin benzologue

F. Fülöp, Márta Palkó, R. Sillanpää, 2000 .

Green Strategies for the Preparation of Enantiomeric 5–8-Membered Carbocyclic β-Amino Acid Derivatives through CALB-Catalyzed Hydrolysis

Sayeh Shahmohammadi, Márta Palkó, E. Forró, 2022, Molecules.

Flow-chemistry enabled efficient synthesis of β-peptides: backbone topology vs. helix formation.

T. Juhász, I. Mándity, S. Béni, 2019, Chemical communications.

Synthesis and Receptor Binding of New Thieno[2,3‐d]‐pyrimidines as Selective Ligands of 5‐HT3 Receptors

G. Maksay, A. Cagnotto, L. Salerno, 2008, Archiv der Pharmazie.

Angular Regioselectivity in the Reactions of 2-Thioxopyrimidin-4-ones and Hydrazonoyl Chlorides: Synthesis of Novel Stereoisomeric Octahydro[1,2,4]triazolo[4,3-a]quinazolin-5-ones

M. Haukka, F. Fülöp, Márta Palkó, 2020, Molecules.

Synthesis and biological evaluation of the new ring system benzo[f]pyrimido[1,2-d][1,2,3]triazolo[1,5-a][1,4]diazepine and its cycloalkane and cycloalkene condensed analogues

M. Haukka, F. Fülöp, I. Zupkó, 2021, RSC advances.

Synthesis of Novel N-Heterocyclic Compounds Containing 1,2,3-Triazole Ring System via Domino, “Click” and RDA Reactions

F. Fülöp, Márta Palkó, Mohamed El Haimer, 2019, Molecules.

Synthesis of mono- and dihydroxy-substituted 2-aminocyclooctanecarboxylic acid enantiomers

F. Fülöp, Márta Palkó, R. Sillanpää, 2010 .

Efficient synthesis of 3,4- and 4,5-dihydroxy-2-amino-cyclohexanecarboxylic acid enantiomers

F. Fülöp, T. Martinek, Márta Palkó, 2009 .

Efficient Synthesis of Hydroxy‐Substituted Cispentacin Derivatives

F. Fülöp, T. Martinek, Márta Palkó, 2008 .

Facile Regio‐ and Diastereoselective Syntheses of Hydroxylated2‐Aminocyclohexanecarboxylic Acids

F. Fülöp, T. Martinek, Márta Palkó, 2005 .

Synthesis and Transformations of di-endo-3-Aminobicyclo-[2.2.2]oct-5-ene-2-carboxylic Acid Derivatives

F. Fülöp, Márta Palkó, P. Sohár, 2011, Molecules.

Comparative study on the liquid chromatographic enantioseparation of cyclic β-amino acids and the related cyclic β-aminohydroxamic acids on Cinchona alkaloid-based zwitterionic chiral stationary phases.

F. Fülöp, M. Kohout, W. Lindner, 2018, Journal of separation science.

Synthesis and Stereostructure of 3-Amino-5- and -6-hydroxybicyclo[2.2.1]heptane-2-carboxylic Acid Diastereomers

F. Fülöp, Márta Palkó, P. Sohár, 2005 .

Sythesis and Retro Diels-Alder Decomposition of 1,4-Methanopyrrolo-,1,4-Methanopyrido- and 1,4-Methanoazepino[2,1-b]-quinazolinones1

F. Fülöp, Márta Palkó, G. Bernáth, 1997 .

Syntheses of Four Enantiomers of 2,3-Diendo- and 3-Endo-aminobicyclo[2.2.2]oct-5-ene-2-exo-carboxylic Acid and Their Saturated Analogues

F. Fülöp, Márta Palkó, R. Sillanpää, 2013, Molecules.

Retro Diels Alder protocol for regioselective synthesis of novel [1,2,4]triazolo[4,3-a]pyrimidin-7(1H)-ones

M. Haukka, F. Fülöp, Márta Palkó, 2020, RSC advances.

Synthesis of Alicyclic 2-Methylenethiazolo[2,3-b]quinazolinone Derivatives via Base-Promoted Cascade Reactions

I. Zupkó, Márta Palkó, Z. Schelz, 2021, Synthesis.

Continuous-Flow retro-Diels-Alder Reaction: A Process Window for Designing Heterocyclic Scaffolds

I. Mándity, F. Fülöp, Márta Palkó, 2018, European Journal of Organic Chemistry.

Structural and temperature effects on enantiomer separations of bicyclo[2.2.2]octane-based 3-amino-2-carboxylic acids on cinchona alkaloid-based zwitterionic chiral stationary phases.

F. Fülöp, W. Lindner, Márta Palkó, 2014, Journal of pharmaceutical and biomedical analysis.

Syntheses of Hydroxylated Cyclic β-Amino Acid Derivatives

F. Fülöp, Márta Palkó, L. Kiss, 2005 .

Enantiomeric separation of bicyclo[2.2.2]octane-based 2-amino-3-carboxylic acids on macrocyclic glycopeptide chiral stationary phases.

D. Armstrong, F. Fülöp, Márta Palkó, 2014, Chirality.

High-performance liquid chromatographic enantioseparation of cyclic β-aminohydroxamic acids on zwitterionic chiral stationary phases based on Cinchona alkaloids.

F. Fülöp, W. Lindner, Beáta Fekete, 2016, Analytica chimica acta.

Continuous-flow retro-Diels–Alder reaction: an efficient method for the preparation of pyrimidinone derivatives

I. Mándity, F. Fülöp, Márta Palkó, 2018, Beilstein journal of organic chemistry.

Synthesis and transformations of stereoisomeric ethyl 2‐isothiocyanato‐1‐cyclopentanecarboxylatesm

F. Evanics, F. Fülöp, Márta Palkó, 2000 .

Novel High Affinity Sigma-1 Receptor Ligands from Minimal Ensemble Docking-Based Virtual Screening

B. Penke, F. Fülöp, Márta Palkó, 2021, International journal of molecular sciences.

Angular Regioselective Synthesis of Varied Functionalized Hexahydro-1,2,4-triazolo[4,3-a]quinazolin-9-ones and Their Antiproliferative Action

M. Haukka, I. Zupkó, Márta Palkó, 2023, Molecules.

Synthesis and stereochemistry of indano[1,2-d][1,3]oxazines and thiazines, new ring systems

F. Fülöp, Márta Palkó, A. Hetényi, 2004 .