Abstract
(Z)- and
(E)-4-Amino-3-(4-chlorophenyl)but-2-enoic acids have been synthesized from
4-chloroacetophenone as conformationally restricted analogues of baclofen. The
corresponding unsaturated lactam (4) has been catalytically reduced and
hydrolysed to baclofen to demonstrate the suitability of (4) as a precursor for
radiolabelled baclofen of high specific activity.
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