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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 2024 Volume 34, Issue 4, Pages 496–498 (Mi mendc165)

This article is cited in 1 paper

Communications

A metal-templated synthesis of precursors for (2S)- and (2R)-2-(3-[18F]fluoropropyl)tyrosines as potential radiotracers for positron emission tomography

T. F. Savel'yeva, Z. T. Gugkaeva, Yu. V. Nelyubina, A. F. Smol'yakov, M. A. Moskalenko, V. A. Larionov, V. I. Maleev

A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation

Abstract: New asymmetric metal-templated synthesis of enantiomers of (2S)- and (2R)-2-(3-[19F]fluoropropyl)tyrosine precursors were obtained based on a chiral NiII complex of the Schiff base derived from (S)-2-[N-(N’-benzylprolyl)amino]-benzaldehyde and racemic tyrosine in five steps. The free tyrosine derivatives which can be obtained upon decomplexation seem promising radiotracers for positron emission tomography imaging provided the introduction of 18F isotope.

Keywords: 18F-labelled amino acids, tyrosine, asymmetric synthesis, nucleophilic substitution, nickel(ii) complexes.

Language: English

DOI: 10.1016/j.mencom.2024.06.008



© Steklov Math. Inst. of RAS, 2025