Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5277038 | Tetrahedron Letters | 2006 | 4 Pages |
Abstract
The efficient use of a polyazamacrocycle as chiral solvating agent (CSA) for the determination of the enantiomeric excess of different carboxylic acids has been studied. All the data agree with the formation of multimolecular diastereomeric complexes in solution, which render good splitting of the NMR signals for the enantiomers of the acids (up to ÎÎδ = 0.20 ppm) using a small amount (even 0.125 equiv) of the receptor.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Almudena González-Álvarez, Ignacio Alfonso, Vicente Gotor,