K. Gyimesi-Forrás

Enantiomer separation of a powerful chiral auxiliary, 2-methoxy-2-(1-naphthyl)propionic acid by liquid chromatography using chiral anion exchanger-type stationary phases in polar-organic mode; investigation of molecular recognition aspects

K. Gyimesi-Forrás, Kazuaki Akasaka, Michael Lämmerhofer et al. · Chirality · 2005 · 37 citations · Full text

Molecular Recognition Aspects, Engineering, Organic Chemistry +17

Investigations of molecular recognition aspects related to the enantiomer separation of 2‐methoxy‐2‐(1‐naphthyl)propionic acid using quinine carbamate as chiral selector: An NMR and FT‐IR spectroscopic as well as X‐ray crystallographic study†

Kazuaki Akasaka, K. Gyimesi-Forrás, Michael Lämmerhofer et al. · Chirality · 2005 · 33 citations

Molecular Recognition Aspects, Engineering, Conformational Transition +16

Comparative study on the use of ortho-phthalaldehyde, naphthalene-2,3-dicarboxaldehyde and anthracene-2,3-dicarboxaldehyde reagents for α-amino acids followed by the enantiomer separation of the formed isoindolin-1-one derivatives using quinine-type chiral stationary phases

K. Gyimesi-Forrás, Alexander Leitner, Kazuaki Akasaka et al. · Journal of Chromatography A · 2005 · 23 citations

Isoindolin-1-one Derivatives, Derivative (Chemistry), Derivatives +9

Enantiomer separation of imidazo‐quinazoline‐dione derivatives on quinine carbamate‐based chiral stationary phase in normal phase mode

K. Gyimesi-Forrás, Norbert M. Maier, József Kökösi et al. · Chirality · 2008 · 17 citations

Enantiomer Separation, Asymmetric Catalysis, Derivatives +15

Evaluation of CD detection in an HPLC system for analysis of DHEA and related steroids

András Gergely, G Szász, A. Szentesi et al. · Analytical and Bioanalytical Chemistry · 2006 · 15 citations

Related Steroids, Medicine, Bioanalysis +7