Enantiomer‐Differentiation Induced by an Enantiomeric Excess during Chromatography with Achiral Phases
- 18 December 1985
- journal article
- research article
- Published by Wiley in Helvetica Chimica Acta
- Vol. 68 (8), 2238-2243
- https://doi.org/10.1002/hlca.19850680818
Abstract
No abstract availableKeywords
This publication has 41 references indexed in Scilit:
- La coupe du roi and its relevance to stereochemistry. Combination of two homochiral molecules to give an achiral productJournal of the American Chemical Society, 1983
- Spezifikation des sterischen Verlaufs von asymmetrischen SynthesenAngewandte Chemie, 1982
- Liquid chromatography on triacetylcellulose, 4. Determination of enantiomeric purity in spite of incomplete chromatographic separationEuropean Journal of Inorganic Chemistry, 1982
- The Stereochemical Outcomes – the Isoborneol/Borneol Ratios – in Lithium, Sodium and Potassium/Ammonia Reductions without a Proton Source of the Enantiomers and the Racemate of Camphor Differ StronglyHelvetica Chimica Acta, 1982
- Aqueous lanthanide shift reagents. 8. Chiral interactions and stereochemical assignments of chemically and isotopically chiral ligandsJournal of the American Chemical Society, 1980
- Étude expérimentale de l'auto‐association des molécules modèles dipeptidiques. II. Association stéréosélective des molécules énantiomèresBiopolymers, 1976
- Methoden der asymmetrischen Synthese – enantioselektive katalytische HydrierungAngewandte Chemie, 1971
- Stereoregulation in N‐carboxy anhydride polymerizationJournal of Polymer Science Part C: Polymer Symposia, 1968
- Asymmetric selection in the copolymerization of N‐carboxy‐L‐ and D‐alanine anhydrideBiopolymers, 1967
- Reaktionen mit Mikroorganismen. 1. Mitteilung. Die stereospezifische Reduktion von (±)‐Δ4‐9‐Methyl‐octalindion‐(3,8)Helvetica Chimica Acta, 1956