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Fast and Efficient 18 F‐Labeling by [ 18 F]Fluorophenylazocarboxylic Esters
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 giv...
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Published in: | Chemistry : a European journal 2014-01, Vol.20 (2), p.370-375 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | 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. |
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ISSN: | 0947-6539 1521-3765 |
DOI: | 10.1002/chem.201303409 |