Exploring the enantiorecognition mechanism of Cinchona alkaloid-based zwitterionic chiral stationary phases and the basic trans-paroxetine enantiomers
The enantiomers of trans-paroxetine (the selectand) were separated on four chiral stationary phases incorporating either quinine [ZWIX(+), ZWIX(+A)] or quinidine [ZWIX(–), ZWIX(–A)] and (R,R)-aminocyclohexanesulfonic acid [in ZWIX(–), and ZWIX(+A)] or (S,S)-aminocyclohexanesulfonic acid [in ZWIX(+),...
Elmentve itt :
| Szerzők: |
Sardella Roccaldo Macchiarulo Antonio Urbinati Fabrizio Ianni Federica Carotti Andrea Kohout Michal Lindner Wolfgang Péter Antal Ilisz István |
|---|---|
| Dokumentumtípus: | Cikk |
| Megjelent: |
2018
|
| Sorozat: | JOURNAL OF SEPARATION SCIENCE
41 No. 6 |
| Tárgyszavak: | |
| doi: | 10.1002/jssc.201701068 |
| mtmt: | 3393167 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/29245 |
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