| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5222747 | Tetrahedron | 2009 | 6 Pages |
Abstract
Schiff-base ligands are often used as backbone ligands for mono- and dinuclear complexes that serve as catalysts during aerobic oxidation reactions. However, their water solubility is low and limits their applicability as catalysts to transform highly water-soluble biomolecules, such as carbohydrates or amino alcohols. A new method to regioselectively incorporate water solubility-promoting polyethylene glycol side chains into a frequently used aldehyde building block of Schiff-base ligands has been developed.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Moses G. Gichinga, Susanne Striegler,