Literature DB >> 21952126

Sultone opening with [18F]fluoride: an efficient 18F-labelling strategy for PET imaging.

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 2011

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Year:  2011        PMID: 21952126     DOI: 10.1039/c1cc14435a

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

Review 1.  Progress in the synthesis of δ-sultones.

Authors:  Christina Gaunersdorfer; Mario Waser
Journal:  Monatsh Chem       Date:  2017-07-15       Impact factor: 1.451

2.  Sultones and Sultines via a Julia-Kocienski Reaction of Epoxides.

Authors:  Geoffrey M T Smith; Paul M Burton; Christopher D Bray
Journal:  Angew Chem Int Ed Engl       Date:  2015-10-27       Impact factor: 15.336

  2 in total

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