Ferenc Bertha
Egis Pharmaceuticals (Hungary)(HU)
Publications by Year
Research Areas
Synthesis of β-Lactam Compounds, Synthesis and Catalytic Reactions, Synthesis and Biological Evaluation, Antibiotics Pharmacokinetics and Efficacy, Crystallization and Solubility Studies
Most-Cited Works
- → Selective NR1/2BN-Methyl-d-aspartate Receptor Antagonists among Indole-2-carboxamides and Benzimidazole-2-carboxamides(2007)43 cited
- → Preparation of a new chiral acridino-18-crown-6 ether-based stationary phase for enantioseparation of racemic protonated primary aralkyl amines(2007)30 cited
- → New practical synthesis of 5-formylindole(2005)26 cited
- → Synthesis of new optically active acridino-18-crown-6 ligands and studies of their potentiometric selectivity toward the enantiomers of protonated 1-phenylethylamine and metal ions(2009)22 cited
- → Benzimidazole-2-carboxamides as novel NR2B selective NMDA receptor antagonists(2006)21 cited
- → Simple and condensed β-lactams. Part 33. AlCl3 catalyzed ring closures of some 3-aryloxy-4-oxoazetidine-2-carboxylic chlorides to 1H-chromeno[3,2-b]azete-2,8(2aH,8aH)-diones and some reactions of the products(1999)19 cited
- → On the anomalous behaviour of (3RS,4RS)-[(2RS)-3-acetylthiazolidin-2-yl]-1-(4-methoxyphenyl)azetidin-2-ones towards cerium(IV) ammonium nitrate (CAN). An unprecedented oxidative ring transformation.(1993)15 cited
- → Simple and condensed β-lactams, part 31. Acid catalyzed ring closures and ring transformations of some 3-aryloxy-4-oxoazetidine-2-carbaldehydes(1998)14 cited
- → Synthesis of new enantiopure proton-ionizable crown ethers containing a dialkylhydrogenphosphate moiety(2006)12 cited
- → Regioselective reactions of mesyloxymethylazetidinones with nucleophiles I. Cleavage of the azetidinone ring, azetidinone‐aziridine ring transformations(2006)10 cited