Data in Brief (Dec 2015)

Smart tools and orthogonal click-like reactions onto small unilamellar vesicles: Additional molecular data

  • Maria Vittoria Spanedda,
  • Christophe Salomé,
  • Benoît Hilbold,
  • Etienne Berner,
  • Béatrice Heurtault,
  • Sylvie Fournel,
  • Benoît Frisch,
  • Line Bourel-Bonnet

DOI
https://doi.org/10.1016/j.dib.2015.08.014
Journal volume & issue
Vol. 5, no. C
pp. 145 – 154

Abstract

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We present here the synthetic routes and the experimental data (NMR and MS spectra) for model reactions for copper-free Huisgen 1,4-cycloaddition, Staudinger ligation and for addition of a dithiol on a dibromomaleimide ring. Starting materials were synthesized from the commercially available 4-chlorophenethylamine, previously described 2-(cyclooct-2-yn-1-yloxy)acetic acid, 1-fluorocyclooct-2-ynecarboxylic acid, commercial 2-(diphenylphosphino)terephthalic acid 1-methyl 4-pentafluorophenyl diester and dibromomaleimide. In all cases, the expected compounds were obtained with good yield (50% to quantitative). A novel synthesis of the lipid anchor DOGP3NH2 is also described. These data were used as basis for the study reported in the article “Smart Tools and Orthogonal Click-like Reactions onto Small Unilamellar Vesicles” in Chemistry and Physics of Lipids [1].