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Biocatalytic Reduction Reactions from a Chemist's Perspective

Reductions play a key role in organic synthesis, producing chiral products with new functionalities. Enzymes can catalyse such reactions with exquisite stereo‐, regio‐ and chemoselectivity, leading the way to alternative shorter classical synthetic routes towards not only high‐added‐value compounds...

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Detalles Bibliográficos
Autores principales: Hollmann, Frank, Opperman, Diederik J., Paul, Caroline E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983917/
https://www.ncbi.nlm.nih.gov/pubmed/32330347
http://dx.doi.org/10.1002/anie.202001876
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author Hollmann, Frank
Opperman, Diederik J.
Paul, Caroline E.
author_facet Hollmann, Frank
Opperman, Diederik J.
Paul, Caroline E.
author_sort Hollmann, Frank
collection PubMed
description Reductions play a key role in organic synthesis, producing chiral products with new functionalities. Enzymes can catalyse such reactions with exquisite stereo‐, regio‐ and chemoselectivity, leading the way to alternative shorter classical synthetic routes towards not only high‐added‐value compounds but also bulk chemicals. In this review we describe the synthetic state‐of‐the‐art and potential of enzymes that catalyse reductions, ranging from carbonyl, enone and aromatic reductions to reductive aminations.
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spelling pubmed-79839172021-03-24 Biocatalytic Reduction Reactions from a Chemist's Perspective Hollmann, Frank Opperman, Diederik J. Paul, Caroline E. Angew Chem Int Ed Engl Reviews Reductions play a key role in organic synthesis, producing chiral products with new functionalities. Enzymes can catalyse such reactions with exquisite stereo‐, regio‐ and chemoselectivity, leading the way to alternative shorter classical synthetic routes towards not only high‐added‐value compounds but also bulk chemicals. In this review we describe the synthetic state‐of‐the‐art and potential of enzymes that catalyse reductions, ranging from carbonyl, enone and aromatic reductions to reductive aminations. John Wiley and Sons Inc. 2020-11-03 2021-03-08 /pmc/articles/PMC7983917/ /pubmed/32330347 http://dx.doi.org/10.1002/anie.202001876 Text en © 2020 The Authors. Published by Wiley-VCH GmbH This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Hollmann, Frank
Opperman, Diederik J.
Paul, Caroline E.
Biocatalytic Reduction Reactions from a Chemist's Perspective
title Biocatalytic Reduction Reactions from a Chemist's Perspective
title_full Biocatalytic Reduction Reactions from a Chemist's Perspective
title_fullStr Biocatalytic Reduction Reactions from a Chemist's Perspective
title_full_unstemmed Biocatalytic Reduction Reactions from a Chemist's Perspective
title_short Biocatalytic Reduction Reactions from a Chemist's Perspective
title_sort biocatalytic reduction reactions from a chemist's perspective
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983917/
https://www.ncbi.nlm.nih.gov/pubmed/32330347
http://dx.doi.org/10.1002/anie.202001876
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