Studies aiming at the synthesis of morphine II

Csaba Szántay, Gábor Blaskó, M. BARCZAI‐BEKE, +2

Tetrahedron Letters

Medicinal ChemistryNatural SciencesMedicineMorphine IiOpioid Overdose +5

New routes to clavine-type ergot alkaloids. Part 2: Synthesis of the last, so far not yet synthesized member of the clavine alkaloid family, (±)-cycloclavine

Mária Incze, Gábor Dörnyei, István Moldvai, +3

Tetrahedron

Diversity Oriented SynthesisNew RoutesBiochemistryNatural SciencesMedicine +7

Synthetic Route to Ergot Alkaloids

István Moldvai, Eszter Temesvári-Major, Mária Incze, +3

Helvetica Chimica Acta

Industrial MycologyBiosynthesisNatural Product SynthesisErgot AlkaloidsBiochemistry +9

Studies aimed at the synthesis of morphine. 3. Synthesis of (.+-.)-salutaridine via phenolic oxidative coupling of (.+-.)-reticuline

Csaba Szántay, M. BARCZAI‐BEKE, Péter Péchy, +2

The Journal of Organic Chemistry

Pharmaceutical ScienceAltmetric Attention ScoreOrganic ChemistryPharmacotherapyPharmaceutical Chemistry +15

Studies aimed at the synthesis of morphine. 7. Biomimetic total synthesis of (.+-.)-pallidine

Gábor Blaskó, Gábor Dörnyei, M. BARCZAI‐BEKE, +2

The Journal of Organic Chemistry

Pharmaceutical ScienceBioorganic ChemistryAltmetric Attention ScoreOrganic ChemistryPharmacotherapy +17

Synthesis of corynantheidine alkaloids—III

M. BARCZAI‐BEKE, Gábor Dörnyei, Gábor Tóth, +2

Tetrahedron

Corynantheidine Alkaloids—iiiOrganic ChemistryPharmacologySynthetic ChemistryNatural Product Synthesis

Synthesis, anti-GABA activity and preferred conformation of bicuculline and norbicuculline enantiomers

Julianna Kardos, Tamás Blandl, N. D. LUYEN, +6

European Journal of Medicinal Chemistry

Norbicuculline EnantiomersBiochemistryOrganic ChemistryPreferred ConformationStereoselective Synthesis +3

Studies on the Synthesis of Morphine VI*

Cs. Szántay, G. BLASKO, M. BARCZAI‐BEKE, +2

Planta Medica

Combinatorial ChemistryMolecular PharmacologyMedicinal ChemistrySystematic InvestigationsBioorganic Chemistry +11

Validation of high-affinity binding sites for succinic acid through distinguishable binding of gamma-hydroxybutyric acid receptor-specific NCS 382 antipodes

Tünde Molnár, Júlia Visy, Ágnes Simon, +5

Bioorganic & Medicinal Chemistry Letters

Molecular DockingMedicinal ChemistryBiochemistryDistinguishable BindingMedicine +9

N‐Aminierung von Isochinolinbasen

Siegfried Andreae, Ernst Schmitz, Helmut Sonnenschein, +3

Journal für praktische Chemie

Indane Derivatives 13BDerivative (Chemistry)HeterocyclicSecondary IsoquinolineNatural Sciences +8