This title appears in the Scientific Report :
2007
Please use the identifier:
http://dx.doi.org/10.1016/j.jorganchem.2007.06.009 in citations.
[18F]fluorophenyl organometallics as intermediates of no-carrier-added 18F-fluoroarylation reactions
[18F]fluorophenyl organometallics as intermediates of no-carrier-added 18F-fluoroarylation reactions
Based on the recent availability of no-carrier-added (n.c.a.) 1-bromo-4-[F-18]fluorobenzene with high radiochemical yield, the 4[F-18]fluorophenyl compounds of lithium, sodium and magnesium can now also effectively be prepared. Thus, [F-18]fluoroarene reagents with a nucleophilic reaction centre are...
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Personal Name(s): | Ermert, J. |
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Ludwig, T. / Gail, R. / Coenen, H. H. | |
Contributing Institute: |
Nuklearchemie; INB-4 |
Published in: | Journal of organometallic chemistry, 692 (2007) S. 4084 - 4092 |
Imprint: |
New York, NY [u.a.]
Elsevier
2007
|
Physical Description: |
4084 - 4092 |
DOI: |
10.1016/j.jorganchem.2007.06.009 |
Document Type: |
Journal Article |
Research Program: |
Funktion und Dysfunktion des Nervensystems |
Series Title: |
Journal of Organometallic Chemistry
692 |
Subject (ZB): | |
Publikationsportal JuSER |
Based on the recent availability of no-carrier-added (n.c.a.) 1-bromo-4-[F-18]fluorobenzene with high radiochemical yield, the 4[F-18]fluorophenyl compounds of lithium, sodium and magnesium can now also effectively be prepared. Thus, [F-18]fluoroarene reagents with a nucleophilic reaction centre are available and suitable among others for the formation of [18F]fluorophenyl compounds with electron donating substituents in the radiosynthesis of F-18-labelled complex organic structures. For these arylation reactions, however, the presence of macroscopic amounts of a haloarene as co-reactant is necessary with all n.c.a. [F-18]fluorophenyl metallics. The F-18-fluoroarylation was verified for examples of aryl-carbon, -silicon, -sulphur, and -nitrogen bond formation with radiochemical yields of 20-25% related to the starting radioactivity of [18 F]fluoride. (c) 2007 Elsevier B.V. All rights reserved. |