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Solid phase synthesis of [18F]labelled peptides for positron emission tomography
J L Sutcliffe-Goulden1, M J O'Doherty, S S Bansal
1Department of Pharmacy, Kings College London, UK.
Bioorganic & Medicinal Chemistry Letters
|July 29, 2000
Abstract:
A strategy for the solid phase synthesis of [18F]labelled peptides has been developed. The peptides were prepared on solid support and acylated with 4-[18F]fluorobenzoic acid using HATU within 3 min and the labelled peptide was released from the solid support within 7 min. The [18F]labelled peptides were produced in good purity with a specific activity of 20-25 GBq/micromol.