| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5263220 | Tetrahedron Letters | 2013 | 4 Pages |
Abstract
Three new chiral urea-type anion receptors were synthesized from aromatic diamines and 1-amino-1-deoxyglucose. The anion binding properties of these receptors were studied using chiral carboxylates derived from mandelic acid and three α-amino acids. We found that the size of the anion binding pocket played an important role in chiral recognition processes. The best results were obtained for 1,8-diaminoanthracene and α-amino acid anions.
Related Topics
Physical Sciences and Engineering
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Authors
Paulina Hamankiewicz, JarosÅaw M. Granda, Janusz Jurczak,