Synthesis of 3-chloro-6-((4-(di-tert-butyl[18F]fluorosilyl)-benzyl)oxy)-1,2,4,5-tetrazine ([18F]SiFA-OTz) for rapid tetrazine-based 18F-radiolabeling

An efficient method to prepare the 18F-labeled tetrazine-derivative [18F]-SiFA-OTz for bioorthogonal radiochemistry was developed. [18F]-SiFA-OTz can be synthesized with a radiochemical yield of 78 ± 5% within 25 min and can quantitatively react with a model strained dienophile, trans-cyclooctenol.

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Bibliographic Details
Main Authors: Zhu, Jun (Author) , Wängler, Carmen (Author) , Wängler, Björn (Author)
Format: Article (Journal)
Language:English
Published: 23 June 2015
In: Chemical communications
Year: 2015, Volume: 51, Issue: 62, Pages: 12415-12418
ISSN:1364-548X
DOI:10.1039/C5CC03623B
Online Access:Verlag, Volltext: http://dx.doi.org/10.1039/C5CC03623B
Verlag, Volltext: http://pubs.rsc.org/en/content/articlelanding/2015/cc/c5cc03623b
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Author Notes:Jun Zhu, Stephen Li, Carmen Wängler, Björn Wängler, R. Bruce Lennox, Ralf Schirrmacher
Description
Summary:An efficient method to prepare the 18F-labeled tetrazine-derivative [18F]-SiFA-OTz for bioorthogonal radiochemistry was developed. [18F]-SiFA-OTz can be synthesized with a radiochemical yield of 78 ± 5% within 25 min and can quantitatively react with a model strained dienophile, trans-cyclooctenol.
Item Description:Gesehen am 31.08.2017
Physical Description:Online Resource
ISSN:1364-548X
DOI:10.1039/C5CC03623B