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

Open Access
Authors
  • E. De Marchi
  • T. Hilberath
  • C. Zippilli
  • R. Wever
  • R. Saladino
  • F. Hollmann
  • L. Botta
Publication date 06-08-2024
Journal Advanced Synthesis and Catalysis
Volume | Issue number 366 | 15
Pages (from-to) 3290-3296
Organisations
  • Faculty of Science (FNWI) - Van 't Hoff Institute for Molecular Sciences (HIMS)
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
Document type Article
Language English
Published at https://doi.org/10.1002/adsc.202400516
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