Author

Gábor Szántó

Observed name: Gabor Szanto

Institution: Gedeon Richter (Hungary)

Observed institutions: Gedeon Richter (Hungary), Budapest University of Technology and Economics, Hungarian Academy of Sciences

ORCID: 0000-0003-2865-2804

Observed ORCID: 0000-0003-2865-2804

OpenAlex ID: A5061681972

An expedient total synthesis of ent-(−)-7-deoxy-trans-dihydronarciclasine

2009 · Gábor Szántó, László Hegedűs, et al. · Tetrahedron · 36

Stereoselective total synthesis of (±)-7-deoxy-trans-dihydronarciclasine, a potent antineoplastic phenanthridone alkaloid

2009 · Gábor Szántó, László Hegedűs, et al. · Tetrahedron Letters · 22

Highly enantioselective organocatalytic conjugate addition of nitromethane to benzylidene acetones

2008 · Gábor Szántó, Petra Bombicz, et al. · Chirality · 12

Stereochemistry of 1,3‐dipolar‐cycloaddition of 3,4‐dihydroisoquinoline‐ and 3,4‐dihydro‐carboline‐N‐methoxycarbonyl‐ and N‐phenacyl‐methylides with maleic and fumaric nitrile

2007 · István Kádas, Gábor Szántó, et al. · Journal of Heterocyclic Chemistry · 11

Discovery of New Heterocyclic Ring Systems as Novel and Potent V1A Receptor Antagonists

2020 · Ferenc Baska, Gábor Szántó, et al. · ACS Chemical Neuroscience · 8

New V1a receptor antagonist. Part 2. Identification and optimization of triazolobenzazepines

2020 · Éva Bozó, Ferenc Baska, et al. · Bioorganic & Medicinal Chemistry Letters · 6

New P2X3 receptor antagonists. Part 2: Identification and SAR of quinazolinones

2016 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 5

New P2X3 receptor antagonists. Part 1: Discovery and optimization of tricyclic compounds

2016 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 5

Hydrogenation of (±)-trans-2-arylnitrocyclohexane derivatives over palladium

2009 · Gábor Szántó, István Kádas, et al. · Reaction Kinetics Mechanisms and Catalysis · 5

Discovery and Characterization of RGH-122, a Potent, Selective, and Orally Bioavailable V1a Receptor Antagonist

2024 · Ferenc Baska, Éva Bozó, et al. · Journal of Medicinal Chemistry · 4

Novel-Type GABAB PAMs: Structure–Activity Relationship in Light of the Protein Structure

2024 · Balázs Krámos, Zsuzsa Hadady, et al. · ACS Medicinal Chemistry Letters · 3

New V1a receptor antagonist. Part 1. Synthesis and SAR development of urea derivatives

2020 · Gábor Szántó, Attila Makó, et al. · Bioorganic & Medicinal Chemistry Letters · 2

Development of dual V1a/V2 antagonists containing triazolobenzazepine scaffold

2024 · Gábor Varró, Éva Bozó, et al. · European Journal of Medicinal Chemistry · 1

ChemInform Abstract: Stereochemistry of 1,3‐Dipolar‐cycloaddition of 3,4‐Dihydroisoquinoline‐ and 3,4‐Dihydro‐carboline‐N‐methoxycarbonyl‐ and N‐Phenacyl‐methylides with Maleic and Fumaric Nitrile.

2008 · Istvan Kadas, Gabor Szanto, et al. · ChemInform

Works count: 14

Citation count: 120

H-index: 6

I10-index: 4