4.7 Article

Bioconjugated arylpalladium complexes on solid supports for a convenient last-step synthesis of 11C-labelled tracers for positron emission tomography

Journal

CHEMICAL COMMUNICATIONS
Volume 55, Issue 53, Pages 7587-7590

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc03215k

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Funding

  1. French Agence Nationale de la Recherche [ANR-15-CE18-0015-01]
  2. Investments for the Future Program [ANR-10-LABX-57]
  3. Agence Nationale de la Recherche (ANR) [ANR-15-CE18-0015] Funding Source: Agence Nationale de la Recherche (ANR)

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Arylpalladium complexes prepared from o-iodobenzylalcohol-biomolecule conjugates and triphenylphosphine linked on polystyrene beads provided convenient supported and stable precursors. These heterogeneous substrates could react smoothly with [C-11] CO, affording the corresponding C-11-labelled bioconjugates with isolated radiochemical yields ranging from 4% to 71%, and excellent radiochemical purities from 86% to >98% after a simple filtration. Thus, this method opens up a new pathway for an easier automation of Pd-catalysed syntheses of PET tracers.

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