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dc.contributor.authorMattey, Ashley P.; orcid: 0000-0002-6564-7150
dc.contributor.authorFord, Grayson J.
dc.contributor.authorCitoler, Joan
dc.contributor.authorBaldwin, Christopher
dc.contributor.authorMarshall, James R.
dc.contributor.authorPalmer, Ryan B.
dc.contributor.authorThompson, Matthew
dc.contributor.authorTurner, Nicholas J.; orcid: 0000-0002-8708-0781
dc.contributor.authorCosgrove, Sebastian C.; orcid: 0000-0001-9541-7201; email: s.cosgrove@keele.ac.uk
dc.contributor.authorFlitsch, Sabine L.; orcid: 0000-0003-3974-646X; email: Sabine.flitsch@manchester.ac.uk
dc.date.accessioned2021-05-20T16:39:35Z
dc.date.available2021-05-20T16:39:35Z
dc.date.issued2021-05-19
dc.date.submitted2021-03-17
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/624626/ange.202103805.pdf?sequence=2
dc.identifierhttps://chesterrep.openrepository.com/bitstream/handle/10034/624626/ange.202103805.xml?sequence=3
dc.identifier.citationAngewandte Chemie
dc.identifier.urihttp://hdl.handle.net/10034/624626
dc.descriptionFrom Wiley via Jisc Publications Router
dc.descriptionHistory: received 2021-03-17, rev-recd 2021-04-12, pub-electronic 2021-05-19
dc.descriptionArticle version: VoR
dc.descriptionPublication status: Published
dc.descriptionFunder: Biotechnology and Biological Sciences Research Council; Id: http://dx.doi.org/10.13039/501100000268; Grant(s): BB/ L013762/1, BB/M027791/1, BB/M02903411, BB/ M028836/1
dc.descriptionFunder: H2020 European Research Council; Grant(s): 788231-ProgrES-ERC-2017-ADG
dc.description.abstractAbstract: A key aim of biocatalysis is to mimic the ability of eukaryotic cells to carry out multistep cascades in a controlled and selective way. As biocatalytic cascades get more complex, reactions become unattainable under typical batch conditions. Here a number of continuous flow systems were used to overcome batch incompatibility, thus allowing for successful biocatalytic cascades. As proof‐of‐principle, reactive carbonyl intermediates were generated in situ using alcohol oxidases, then passed directly to a series of packed‐bed modules containing different aminating biocatalysts which accordingly produced a range of structurally distinct amines. The method was expanded to employ a batch incompatible sequential amination cascade via an oxidase/transaminase/imine reductase sequence, introducing different amine reagents at each step without cross‐reactivity. The combined approaches allowed for the biocatalytic synthesis of the natural product 4O‐methylnorbelladine.
dc.languageen
dc.rightsLicence for VoR version of this article: http://creativecommons.org/licenses/by/4.0/
dc.sourceissn: 0044-8249
dc.sourceissn: 1521-3757
dc.subjectForschungsartikel
dc.subjectbiocatalytic cascades
dc.subjectcontinuous flow
dc.subjectoxidation
dc.subjectreductive amination
dc.subjecttransamination
dc.titleDevelopment of Continuous Flow Systems to Access Secondary Amines Through Previously Incompatible Biocatalytic Cascades
dc.typearticle
dc.date.updated2021-05-20T16:39:35Z


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