Chemoenzymatic method for the synthesis of enantiomerically pure fluorine-substituted β-methylphenylethylamines

A synthetic approach has been developed leading to the synthesis of new building blocks – enantiomerically pure fluorine-substituted β-methylphenylethylamines. A methodology of kinetic dynamic enzymatic resolution was employed at key stages. A dual enzymatic purification method was applied to achieve a high degree of optical purity of the obtained products. The resulting amines are promising building blocks for developing new pharmaceuticals and physiologically active compounds

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Publication Details

Journal
Ukrainica Bioorganica Acta
Published
2024-12-30
DOI
https://doi.org/10.15407/bioorganica2024.02.003
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00

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article

Chemoenzymatic method for the synthesis of enantiomerically pure fluorine-substituted β-methylphenylethylamines

Anastasy О. Kolodiazhna, Olga O. Kolodiazhna, Oleh O. Faiziiev
Ukrainica Bioorganica Acta
Enzyme Catalysis and Immobilization
article

Chemoenzymatic method for the synthesis of enantiomerically pure fluorine-substituted β-methylphenylethylamines

Anastasy О. Kolodiazhna, Olga O. Kolodiazhna, Oleh O. Faiziiev
article en

Abstract

A synthetic approach has been developed leading to the synthesis of new building blocks – enantiomerically pure fluorine-substituted β-methylphenylethylamines. A methodology of kinetic dynamic enzymatic resolution was employed at key stages. A dual enzymatic purification method was applied to achieve a high degree of optical purity of the obtained products. The resulting amines are promising building blocks for developing new pharmaceuticals and physiologically active compounds

Ukrainica Bioorganica ActaVol. 19(2)
Institute of Bioorganic Chemistry and Petrochemistry V.P. Kukhar (UA)
Enamine
Openalex Percentile: Top 78%
Enzyme Catalysis and Immobilization
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