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Hexafluoroacetone as a protecting and activating reagent: Synthesis of new types of fluoro-substituted α-amino, α-hydroxy and α-mercapto acids

  • Sergej N. Osipov
  • , Torsten Lange
  • , Pavel Tsouker
  • , Jan Spengler
  • , Lothar Hennig
  • , Beate Koksch
  • , Stefan Berger
  • , Salah M. El-Kousy
  • , Klaus Burger

Research output: Contribution to journalArticlepeer-review

18 Scopus citations

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 languageEnglish
Pages (from-to)1821-1829
Number of pages9
JournalSynthesis
Issue number11
DOIs
StatePublished - 3 Aug 2004
Externally publishedYes

Keywords

  • Amino acids
  • Fluorine
  • Hydroxy acids
  • Mercapto acids
  • Peptides

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