Fast and efficient 18F-labeling by [18F]fluorophenylazocarboxylic esters

Fehler S, Maschauer S, Höfling S, Bartuschat A, Tschammer N, Hübner H, Gmeiner P, Prante O, Heinrich M (2014)


Publication Language: English

Publication Type: Journal article, Original article

Publication year: 2014

Journal

Publisher: Wiley-VCH Verlag

Book Volume: 20

Pages Range: 370-375

Journal Issue: 2

DOI: 10.1002/chem.201303409

Abstract

Introduction of [(18) F]fluoride ion into the aromatic core of phenylazocarboxylic esters was achieved in only 30 seconds, with radiochemical yields of up to 95 % (85(±10) %). For labeling purposes, the resulting (18) F-substituted azoester can be further converted in radical-arylation reactions to give biaryls, or in substitutions at its carbonyl unit to produce azocarboxamides. Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

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APA:

Fehler, S., Maschauer, S., Höfling, S., Bartuschat, A., Tschammer, N., Hübner, H.,... Heinrich, M. (2014). Fast and efficient 18F-labeling by [18F]fluorophenylazocarboxylic esters. Chemistry - A European Journal, 20(2), 370-375. https://doi.org/10.1002/chem.201303409

MLA:

Fehler, Stefanie, et al. "Fast and efficient 18F-labeling by [18F]fluorophenylazocarboxylic esters." Chemistry - A European Journal 20.2 (2014): 370-375.

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