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Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis

Vanadate‐dependent chloroperoxidase from Curvularia inaequalis catalyzes 5‐endo‐trig bromocyclizations of α‐allenols to produce valuable halofunctionalized furans as versatile synthetic building blocks. In contrast to other haloperoxidases, also the more challenging 5‐exo‐trig halocyclizations of γ‐...

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Detalles Bibliográficos
Autores principales: Naapuri, Janne M., Wagner, Philip K., Hollmann, Frank, Deska, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734111/
https://www.ncbi.nlm.nih.gov/pubmed/34981903
http://dx.doi.org/10.1002/open.202100236
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author Naapuri, Janne M.
Wagner, Philip K.
Hollmann, Frank
Deska, Jan
author_facet Naapuri, Janne M.
Wagner, Philip K.
Hollmann, Frank
Deska, Jan
author_sort Naapuri, Janne M.
collection PubMed
description Vanadate‐dependent chloroperoxidase from Curvularia inaequalis catalyzes 5‐endo‐trig bromocyclizations of α‐allenols to produce valuable halofunctionalized furans as versatile synthetic building blocks. In contrast to other haloperoxidases, also the more challenging 5‐exo‐trig halocyclizations of γ‐allenols succeed with this system even though the scope still remains more narrow. Benefitting from the vanadate chloroperoxidase‘s high resiliency towards oxidative conditions, cyclization‐inducing reactive hypohalite species are generated in situ from bromide salts and hydrogen peroxide. Crucial requirements for high conversions are aqueous biphasic emulsions as reaction media, stabilized by either cationic or non‐ionic surfactants.
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spelling pubmed-87341112022-01-11 Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis Naapuri, Janne M. Wagner, Philip K. Hollmann, Frank Deska, Jan ChemistryOpen Research Articles Vanadate‐dependent chloroperoxidase from Curvularia inaequalis catalyzes 5‐endo‐trig bromocyclizations of α‐allenols to produce valuable halofunctionalized furans as versatile synthetic building blocks. In contrast to other haloperoxidases, also the more challenging 5‐exo‐trig halocyclizations of γ‐allenols succeed with this system even though the scope still remains more narrow. Benefitting from the vanadate chloroperoxidase‘s high resiliency towards oxidative conditions, cyclization‐inducing reactive hypohalite species are generated in situ from bromide salts and hydrogen peroxide. Crucial requirements for high conversions are aqueous biphasic emulsions as reaction media, stabilized by either cationic or non‐ionic surfactants. John Wiley and Sons Inc. 2022-01-04 /pmc/articles/PMC8734111/ /pubmed/34981903 http://dx.doi.org/10.1002/open.202100236 Text en © 2022 The Authors. Published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Naapuri, Janne M.
Wagner, Philip K.
Hollmann, Frank
Deska, Jan
Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title_full Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title_fullStr Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title_full_unstemmed Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title_short Enzymatic Bromocyclization of α‐ and γ‐Allenols by Chloroperoxidase from Curvularia inaequalis
title_sort enzymatic bromocyclization of α‐ and γ‐allenols by chloroperoxidase from curvularia inaequalis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8734111/
https://www.ncbi.nlm.nih.gov/pubmed/34981903
http://dx.doi.org/10.1002/open.202100236
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