1.
Bioorg Med Chem Lett
; 10(14): 1501-3, 2000 Jul 17.
Article
in English
| MEDLINE
| ID: mdl-10915036
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.
