Synthesis of Enantiopure Vicinal Halohydrins Using a Sequence of Haloperoxidase and Lipase

Journal Article (2024)
Author(s)

Elisa De Marchi (Universita degli Studi della Tuscia Viterbo)

T. Hilberath (TU Delft - BT/Biocatalysis)

Claudio Zippilli (Universita degli Studi della Tuscia Viterbo)

Ron Wever (Universiteit van Amsterdam)

Raffaele Saladino (Universita degli Studi della Tuscia Viterbo)

F. Hollmann (TU Delft - BT/Biocatalysis)

Lorenzo Botta (Universita degli Studi della Tuscia Viterbo)

Research Group
BT/Biocatalysis
DOI related publication
https://doi.org/10.1002/adsc.202400516
More Info
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Publication Year
2024
Language
English
Research Group
BT/Biocatalysis
Issue number
15
Volume number
366
Pages (from-to)
3290-3296
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Abstract

Vicinal halohydrins are key building blocks to produce bioactive molecules and drugs, especially if they can be obtained in enantiomerically pure form. In this study, we present a bi-enzymatic sequence that allows to obtain vic-halohydrins through a photochemoenzymatic olefin hydroxy halogenation followed by a lipase catalysed kinetic resolution. The absolute configuration of the resulting products was determined using Mosher's method.