Racemization, enantiomerization, diastereomerization, and epimerization: Their meaning and pharmacological significance
- 1 January 1995
- Vol. 7 (6) , 396-400
- https://doi.org/10.1002/chir.530070603
Abstract
No abstract availableKeywords
This publication has 12 references indexed in Scilit:
- Enantiomerization of 2,2′‐diisopropylbiphenyl during chiral inclusion gas chromatography: Determination of the rotational energy barrier by computer simulation of dynamic chromatographic elution profilesChirality, 1994
- The so‐called “interconversion” of stereoisomeric drugs: An attempt at clarificationChirality, 1993
- Commonly used chiral drugs: A surveyChirality, 1993
- Determination of enantiomerization barriers by computer simulation of interconversion profiles: enantiomerization of diaziridines during chiral inclusion gas chromatographyJournal of the American Chemical Society, 1992
- cis-trans-Isomerization of [E]-5-(2-bromovinyl)-2,2′-anhydrouridinein vivoin ratsXenobiotica, 1991
- Modelling the Metabolic Epimerization of Anti‐inflammatory 2‐Arylpropanoyl‐coenzyme‐A Conjugates: Solvent effects on the 1H/2H exchange in S‐[2‐(dimethylamino)ethyl] 2‐phenylpropanethioateHelvetica Chimica Acta, 1989
- The metabolic chiral inversion of 2-arylpropionic acids—a novel route with pharmacological consequencesJournal of Pharmacy and Pharmacology, 1983
- Extending the scope of enantiomer resolution by complexation gas chromatographyJournal of the American Chemical Society, 1982
- Proton Magnetic Resonance Investigation of Inversion at Tervalent Nitrogen, 6. Preparative Separations of Enantiomeric Diaziridines by Liquid Chromatography on Triacetylcellulose. Racemizations Monitored by Polarimetry and by 1H NMREuropean Journal of Inorganic Chemistry, 1979
- 362. Aliphatic substitution and the Walden inversion. Part IJournal of the Chemical Society, 1935