Abstract
Starting from (S)-aspartic, (S)-malic, (S)-citramalic and (S,R)-thiomalic acid, new types of 4,4-difluoro-substituted α-amino-, α-hydroxy- and α-mercaptopentanoic acids have been synthesized, applying hexafluoroacetone as protecting and activating reagent. The new partially fluorinated α-functionalized carboxylic acids represent interesting monomers for peptide and depsipeptide modification and for rational design and elucidation of secondary structure.
| Original language | English |
|---|---|
| Pages (from-to) | 1821-1829 |
| Number of pages | 9 |
| Journal | Synthesis |
| Issue number | 11 |
| DOIs | |
| State | Published - 3 Aug 2004 |
| Externally published | Yes |
Keywords
- Amino acids
- Fluorine
- Hydroxy acids
- Mercapto acids
- Peptides
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