A transaminase-mediated aldol reaction and applications in cascades to styryl pyridines-Reference-Cited by-同舟云学术

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A transaminase-mediated aldol reaction and applications in cascades to styryl pyridines

Published:2024 Issue:9 Volume:14 Page:2390-2399
ISSN:2044-4753
Container-title:Catalysis Science & Technology
language:en
Short-container-title:Catal. Sci. Technol.

Author:

Wang Yu¹^ORCID,Li Yiwen²,Ni Yeke¹,Bučar Dejan-Krešimir¹^ORCID,Dalby Paul A.²^ORCID,Ward John M.²^ORCID,Jeffries Jack W. E.²^ORCID,Hailes Helen C.¹^ORCID

Affiliation:

1. Department of Chemistry, University College London, 20 Gordon Street, London, WC1H 0AJ, UK

2. Department of Biochemical Engineering, University College London, Gower Street, London, WC1E 6BT, UK

Abstract

A transaminase mediated aldolase reactivity has been discovered and used to construct styryl pyridines via the use of enzyme cascades.

Funder

Biotechnology and Biological Sciences Research Council

National Institutes of Health

National Institute of Allergy and Infectious Diseases

Publisher

Royal Society of Chemistry (RSC)

Link

http://pubs.rsc.org/en/content/articlepdf/2024/CY/D3CY01370G

Reference45 articles.

1. Recent advances in enzyme promiscuity

2. Stereoselective Promiscuous Reactions Catalyzed by Lipases

3. Biocatalytic promiscuity: the first lipase-catalysed asymmetric aldol reaction

4. Characterization and mechanism insight of accelerated catalytic promiscuity of Sulfolobus tokodaii (ST0779) peptidase for aldol addition reaction

5. Conversion of a PLP-Dependent Racemase into an Aldolase by a Single Active Site Mutation

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