Journal article

Fluorination of an arylboronic ester using [18F]selectfluor bis(triflate): Application to 6-[18F]fluoro-l-DOPA

Abstract:: The Ag-mediated electrophilic [18F]fluorination of an arylboronic ester is reported. This new radiochemical transformation uses [ 18F]selectfluor bis(triflate) in acetone. The process gave 6-[ 18F]fluoro-l-DOPA with a RCY of 19 ± 12% and a specific activity of 2.6 ± 0.3 GBq μmol-1. © 2013 The Royal Society of Chemistry.

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APA Style

Stenhagen, I., Kirjavainen, A., Forsback, S., Jørgensen, C., Robins, E., Luthra, S., Solin, O., & Gouverneur, V. (2013). Fluorination of an arylboronic ester using [18F]selectfluor bis(triflate): Application to 6-[18F]fluoro-l-DOPA. Chemical Communications, 49(14), 1386–1388.

MLA Style

Stenhagen, I., et al. “Fluorination of an Arylboronic Ester Using [18F]Selectfluor Bis(Triflate): Application to 6-[18F]Fluoro-l-DOPA.” Chemical Communications, vol. 49, no. 14, 2013, pp. 1386–88.

Chicago Style

Stenhagen, I, A Kirjavainen, S Forsback, C Jørgensen, E Robins, S Luthra, O Solin, and V Gouverneur. 2013. “Fluorination of an Arylboronic Ester Using [18F]Selectfluor Bis(Triflate): Application to 6-[18F]Fluoro-l-DOPA.” Chemical Communications 49 (14): 1386–88.
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Publisher copy:: 10.1039/c2cc38646a

Authors

+ Stenhagen, I More by this author

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+ Kirjavainen, A More by this author

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+ Forsback, S More by this author

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+ Jørgensen, C More by this author

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+ Robins, E More by this author

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Journal:: Chemical Communications More from this journal
Volume:: 49
Issue:: 14
Pages:: 1386-1388
Publication date:: 2013-02-18
DOI:: 10.1039/c2cc38646a
EISSN:: 1364-548X
ISSN:: 1359-7345

Language:: English
Pubs id:: pubs:379431
UUID:: uuid:eb741aec-76bd-4eaf-b72d-1e4a0a35f949
Local pid:: pubs:379431
Source identifiers:: 379431
Deposit date:: 2013-11-16

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Copyright date:: 2013

Licence:: Terms and Conditions of Use for Oxford University Research Archive

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