| Literature DB >> 21952126 |
Sébastien Schmitt1, Cédric Bouteiller, Louisa Barré, Cécile Perrio.
Abstract
Sultones were subject to ring opening by nucleophilic attack with [(18)F]fluoride to afford easily purified (18)F-labelled hydrophilic sulfonated products in high yields. A two-step sequence including radiofluorination and coupling to lysine was then developed from a bis-sultone precursor as a model approach for the labelling of biopolymers. This journal is © The Royal Society of Chemistry 2011Entities:
Mesh:
Substances:
Year: 2011 PMID: 21952126 DOI: 10.1039/c1cc14435a
Source DB: PubMed Journal: Chem Commun (Camb) ISSN: 1359-7345 Impact factor: 6.222