| Literature DB >> 32391930 |
Thomas C Wilson1, Nagavarakishore Pillarsetty1,2, Thomas Reiner1,2,3.
Abstract
In this paper, we disclose a new strategy for the radiosynthesis of [18 F]PARPi from the corresponding, boc-protected, nitro-precursor. Using a two-step procedure, [18 F]PARPi could be isolated in radiochemical yields up to 9.6%. The reaction proceeds via an efficient one-pot, two-step process, allowing for simplification over previous methods that require complex multi-step, multi-pot strategies to be implemented.Entities:
Keywords: Olaparib; PARP inhibitor; PET chemistry; [18F]PARPi; fluorine-18; radiochemistry
Year: 2020 PMID: 32391930 PMCID: PMC7551923 DOI: 10.1002/jlcr.3847
Source DB: PubMed Journal: J Labelled Comp Radiopharm ISSN: 0362-4803 Impact factor: 1.921