@article{d7718d4143eb41ef869e55685124ad1a,
title = "Radiochemical 18F-fluoroarylation of unsaturated α-, β- and γ-amino acids, application to a radiolabelled analogue of baclofen",
abstract = "Unsaturated α-, β- and γ-amino acids have been investigated as substrates for the reductive Meerwein arylation. Radical reactions of this type have been shown to be a valuable tool for the fast and efficient introduction of the 4-[18F]fluorophenyl group into precursor molecules allowing short-time syntheses of potential PET radiotracers, which would be more difficult to access by other methods.",
author = "H{\"o}fling, {Sarah B.} and Christina Hultsch and Wester, {Hans J{\"u}rgen} and Heinrich, {Markus R.}",
note = "Funding Information: This work was financed by the Fonds der Chemischen Industrie (Liebig fellowship) and the Leonhard-Lorenz-Stiftung. The support of Prof. Dr. Thorsten Bach (TU M{\"u}nchen) and his group is gratefully acknowledged. ",
year = "2008",
month = dec,
day = "22",
doi = "10.1016/j.tet.2008.07.117",
language = "English",
volume = "64",
pages = "11846--11851",
journal = "Tetrahedron",
issn = "0040-4020",
publisher = "Elsevier Ltd.",
number = "52",
}