| Literature DB >> 32612311 |
Stephen Thompson1, So Jeong Lee1, Isaac M Jackson1, Naoko Ichiishi2, Allen F Brooks1, Melanie S Sanford2, Peter J H Scott1.
Abstract
This communication reports a method for the vinylogous radiofluorination of α-diazoacetates to generate γ-[18F]fluoro-α,β-unsaturated esters and ketones in moderate to good radiochemical yields. The method uses no-carrier-added [18F]AgF and is compatible with aromatic and non-aromatic substrates and a number of different functional groups. The labeling method is showcased in the synthesis of a fluorinated 5-cholesten-3-one derivative as well as a difluorinated product pertinent to drug discovery.Entities:
Keywords: Fluorine-18; PET radiochemistry; diazonium chemistry; late-stage fluorination; positron emission tomography
Year: 2019 PMID: 32612311 PMCID: PMC7328919 DOI: 10.1055/s-0039-1690012
Source DB: PubMed Journal: Synthesis (Stuttg) ISSN: 0039-7881 Impact factor: 3.157