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Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule

Supramolecular capsules can be used to change the activity and selectivity of a catalyst through the influence of the second coordination sphere, reminiscent of how enzymes control the selectivity of their processes. In enzymes, this approach is used to also control the enantioselectivity of reactio...

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Detalles Bibliográficos
Autores principales: Jongkind, Lukas J., Reek, Joost N. H.
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/PMC7155075/
https://www.ncbi.nlm.nih.gov/pubmed/32020766
http://dx.doi.org/10.1002/asia.201901771
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author Jongkind, Lukas J.
Reek, Joost N. H.
author_facet Jongkind, Lukas J.
Reek, Joost N. H.
author_sort Jongkind, Lukas J.
collection PubMed
description Supramolecular capsules can be used to change the activity and selectivity of a catalyst through the influence of the second coordination sphere, reminiscent of how enzymes control the selectivity of their processes. In enzymes, this approach is used to also control the enantioselectivity of reactions in which the active catalytic site is often not chiral but the second coordination sphere is. We are interested in the possibility to generate a chiral second coordination sphere around an otherwise achiral transition metal complex for asymmetric catalysis. In this paper we show that the ligand template approach can be used to generate a chiral second coordination sphere around a rhodium complex, which is used in asymmetric hydroformylation.
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spelling pubmed-71550752020-04-15 Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule Jongkind, Lukas J. Reek, Joost N. H. Chem Asian J Full Papers Supramolecular capsules can be used to change the activity and selectivity of a catalyst through the influence of the second coordination sphere, reminiscent of how enzymes control the selectivity of their processes. In enzymes, this approach is used to also control the enantioselectivity of reactions in which the active catalytic site is often not chiral but the second coordination sphere is. We are interested in the possibility to generate a chiral second coordination sphere around an otherwise achiral transition metal complex for asymmetric catalysis. In this paper we show that the ligand template approach can be used to generate a chiral second coordination sphere around a rhodium complex, which is used in asymmetric hydroformylation. John Wiley and Sons Inc. 2020-02-21 2020-03-16 /pmc/articles/PMC7155075/ /pubmed/32020766 http://dx.doi.org/10.1002/asia.201901771 Text en © 2020 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-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Full Papers
Jongkind, Lukas J.
Reek, Joost N. H.
Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title_full Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title_fullStr Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title_full_unstemmed Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title_short Asymmetric Hydroformylation Using a Rhodium Catalyst Encapsulated in a Chiral Capsule
title_sort asymmetric hydroformylation using a rhodium catalyst encapsulated in a chiral capsule
topic Full Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155075/
https://www.ncbi.nlm.nih.gov/pubmed/32020766
http://dx.doi.org/10.1002/asia.201901771
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