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K-Oxyma: A strong acylation-promoting, 2-ctc resin-friendly coupling additive

  • Prabhakar Cherkupally
  • , Gerardo A. Acosta
  • , Lidia Nieto-Rodriguez
  • , Jan Spengler
  • , Hortensia Rodriguez
  • , Sherine N. Khattab
  • , Ayman El-Faham
  • , Marina Shamis
  • , Yoav Luxembourg
  • , Rafel Prohens
  • , Ramon Subiros-Funosas
  • , Fernando Albericio
  • Institute for Research in Biomedicine
  • University of KwaZulu-Natal
  • University of Barcelona
  • Faculty of Science
  • King Saud University
  • Luxembourg Bio Technologies Ltd.
  • Humboldt University of Berlin

Research output: Contribution to journalArticlepeer-review

35 Scopus citations

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 languageEnglish
Pages (from-to)6372-6378
Number of pages7
JournalEuropean Journal of Organic Chemistry
Issue number28
DOIs
StatePublished - Oct 2013
Externally publishedYes

Keywords

  • Acid-labile solid supports
  • Acylation
  • Peptides
  • Solid-phase synthesis

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