Abstract
Here we present a new formulation of the recently introduced OxymaPure additive for peptide bond formation, in which the N-hydroxylamine group is replaced by a potassium salt. The complete suppression of its acidity converts K-Oxyma into the most suitable coupling choice when peptides are assembled on highly acid-labile solid-supports. The coupling efficiency and diminished prospects for epimerization are conserved relative to OxymaPure. In addition, K-Oxyma displays excellent solubility in a variety of organic solvents and undergoes safer decomposition than classical 1-hydroxybenzotriazole additives. A new oxime-based coupling additive is introduced for peptide bond formation. The potassium salt of OxymaPure, K-Oxyma, is readily obtained from commercially available precursors. Unlike common N-hydroxylamines, K-Oxyma is compatible with extremely acid-labile solid-supports, displays excellent solubility, minimizes epimerization, and enhances coupling efficiency relative to OxymaPure.
| Original language | English |
|---|---|
| Pages (from-to) | 6372-6378 |
| Number of pages | 7 |
| Journal | European Journal of Organic Chemistry |
| Issue number | 28 |
| DOIs | |
| State | Published - Oct 2013 |
| Externally published | Yes |
Keywords
- Acid-labile solid supports
- Acylation
- Peptides
- Solid-phase synthesis
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