English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Silver-Mediated 18F-Labeling of Aryl-CF3 and Aryl-CHF2 with 18F-Fluoride

MPS-Authors
/persons/resource/persons207366

Tredwell,  Mathew
University of Oxford, Chemistry Research laboratory, 12 Mansfield Road, OX1 3TA, Oxford, UK ;
Research Group Tredwell, Max-Planck-Institut für Kohlenforschung, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)
There are no public fulltexts stored in PuRe
Supplementary Material (public)
There is no public supplementary material available
Citation

Verhoog, S., Pfeifer, L., Khotavivattana, T., Calderwood, S., Collier, T. L., Wheelhouse, K., et al. (2016). Silver-Mediated 18F-Labeling of Aryl-CF3 and Aryl-CHF2 with 18F-Fluoride. Synlett, 27(1), 25-28. doi:10.1055/s-0035-1560592.


Cite as: https://hdl.handle.net/11858/00-001M-0000-002D-B100-4
Abstract
We report the synthesis of [18F]arylCF3 and [18F]arylCHF2 derivatives from arylCF2Br and arylCHFCl precursors applying a silver-mediated halogen exchange with [18F]fluoride. In the absence of Ag(I)OTf, no reaction takes place at room temperature for both classes of substrates; this result demonstrates the beneficial role of silver(I) as a means to induce 18F-incorporation under very mild conditions.