Acetophenone-based linker for solid-phase peptide synthesis

J Pept Sci. 2000 Feb;6(2):49-56. doi: 10.1002/(SICI)1099-1387(200002)6:2<49::AID-PSC239>3.0.CO;2-6.

Abstract

A new and cost-effective linker for the generation of carboxylic acid end groups on Multipin supports (SynPhase crowns) has been developed. Synthesis of the linker was based on modification of grafted polystyrene (PS) crowns to generate a hydroxyethyl moiety which is acid labile in 10-20% trifluoroacetic acid (TFA) in dichloromethane (DCM). Solid-phase syntheses of model decapeptides using this linker are described.

MeSH terms

  • Acetophenones / chemistry*
  • Chromatography, High Pressure Liquid
  • Ethers, Cyclic / chemistry
  • Methylene Chloride / chemistry
  • Molecular Structure
  • Peptides / chemical synthesis*
  • Polystyrenes / chemistry
  • Spectroscopy, Fourier Transform Infrared
  • Trifluoroacetic Acid / chemistry

Substances

  • Acetophenones
  • Ethers, Cyclic
  • Peptides
  • Polystyrenes
  • Methylene Chloride
  • Trifluoroacetic Acid
  • acetophenone