Article
Cinchona Alkaloid Induced Chiral Discrimination for the Determination of the Enantiomeric Composition of α-Trifluoromethylated Hydroxyl Compounds by 19F NMR Spectroscopy
Tetrahedron: Asymmetry
(2005)
Abstract
The determination of the enantiomeric composition of α-trifluoromethylated-hydroxyl compounds using cinchona alkaloids as chiral selectors is described. The interaction between the alkaloid and trifluoromethylated-hydroxyl compounds converted the enantiotopic nuclei to diastereotopic nuclei observed by 19F NMR spectroscopy. A wide variety of target molecules have been studied to highlight the broad applicability of the method.
Keywords
- Of α-trifluoromethylated-hydroxyl,
- Cinchona alkaloids,
- NMR spectroscopy
Disciplines
Publication Date
2005
Citation Information
Abid Shaikh and Béla Török. "Cinchona Alkaloid Induced Chiral Discrimination for the Determination of the Enantiomeric Composition of α-Trifluoromethylated Hydroxyl Compounds by 19F NMR Spectroscopy" Tetrahedron: Asymmetry Vol. 16 Iss. 8 (2005) Available at: http://works.bepress.com/abid_shaikh/17/