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Synfacts 2011(5): 0466-0466
DOI: 10.1055/s-0030-1259766
DOI: 10.1055/s-0030-1259766
Synthesis of Natural Products and Potential Drugs
© Georg Thieme Verlag
Stuttgart ˙ New York
Synthesis of Kynurenine 3-Hydroxylase Inhibitor FCE28833
T. Jousseaume, N. E. Wurz, F. Glorius*
Universität Münster, Germany
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
15. April 2011 (online)
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Significance
FCE28833 inhibits kynurenine 3-hydroxylase thereby elevating levels of kynurenic acid, an endogenous excitatory amino acid receptor antagonist. It may have therapeutic value in treating diseases linked to hyperfunction of excitatory amino acid receptors. A short and highly enantioselective synthesis of FCE28833 features an asymmetric intermolecular Stetter reaction catalyzed by the N-heterocyclic carbene E.