| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5286365 | Tetrahedron Letters | 2005 | 5 Pages |
Abstract
The synthesis and binding properties of a new class of amino pyrrole based receptors 2 for carboxylates are described. The reversal of the direction of the amide group changes both substrate selectivity and binding affinity relative to known guanidiniocarbonyl pyrrole receptors of type 1 derived from pyrrole-2,5-dicarboxylates.
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Authors
Carsten Schmuck, Jürgen Dudaczek,