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Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles

Herein we report the biocatalytic synthesis of substituted pyrazines and pyrroles using a transaminase (ATA) to mediate the key amination step of the ketone precursors. Treatment of α‐diketones with ATA‐113 in the presence of a suitable amine donor yielded the corresponding α‐amino ketones which und...

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Detalles Bibliográficos
Autores principales: Xu, Jin, Green, Anthony P., Turner, Nicholas J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391939/
https://www.ncbi.nlm.nih.gov/pubmed/30335228
http://dx.doi.org/10.1002/anie.201810555
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author Xu, Jin
Green, Anthony P.
Turner, Nicholas J.
author_facet Xu, Jin
Green, Anthony P.
Turner, Nicholas J.
author_sort Xu, Jin
collection PubMed
description Herein we report the biocatalytic synthesis of substituted pyrazines and pyrroles using a transaminase (ATA) to mediate the key amination step of the ketone precursors. Treatment of α‐diketones with ATA‐113 in the presence of a suitable amine donor yielded the corresponding α‐amino ketones which underwent oxidative dimerization to the pyrazines. Selective amination of α‐diketones in the presence of β‐keto esters afforded substituted pyrroles in a biocatalytic equivalent of the classical Knorr pyrrole synthesis. Finally we have shown that pyrroles can be prepared by internal amine transfer catalyzed by a transaminase in which no external amine donor is required.
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spelling pubmed-63919392019-03-07 Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles Xu, Jin Green, Anthony P. Turner, Nicholas J. Angew Chem Int Ed Engl Communications Herein we report the biocatalytic synthesis of substituted pyrazines and pyrroles using a transaminase (ATA) to mediate the key amination step of the ketone precursors. Treatment of α‐diketones with ATA‐113 in the presence of a suitable amine donor yielded the corresponding α‐amino ketones which underwent oxidative dimerization to the pyrazines. Selective amination of α‐diketones in the presence of β‐keto esters afforded substituted pyrroles in a biocatalytic equivalent of the classical Knorr pyrrole synthesis. Finally we have shown that pyrroles can be prepared by internal amine transfer catalyzed by a transaminase in which no external amine donor is required. John Wiley and Sons Inc. 2018-11-21 2018-12-17 /pmc/articles/PMC6391939/ /pubmed/30335228 http://dx.doi.org/10.1002/anie.201810555 Text en © 2018 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. 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 Communications
Xu, Jin
Green, Anthony P.
Turner, Nicholas J.
Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title_full Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title_fullStr Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title_full_unstemmed Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title_short Chemo‐Enzymatic Synthesis of Pyrazines and Pyrroles
title_sort chemo‐enzymatic synthesis of pyrazines and pyrroles
topic Communications
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6391939/
https://www.ncbi.nlm.nih.gov/pubmed/30335228
http://dx.doi.org/10.1002/anie.201810555
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