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Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag

Water-soluble dendritic iridium catalysts were synthesized by attaching a reactive metal complex to DAB-Am dendrimers via an adapted asymmetric bipyridine ligand. These dendritic catalysts were applied in the aqueous reductive amination of valine while contained in a dialysis bag. Comparable convers...

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Autores principales: Willemsen, Jorgen S, van Hest, Jan C M, Rutjes, Floris P J T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Beilstein-Institut 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678615/
https://www.ncbi.nlm.nih.gov/pubmed/23766812
http://dx.doi.org/10.3762/bjoc.9.110
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author Willemsen, Jorgen S
van Hest, Jan C M
Rutjes, Floris P J T
author_facet Willemsen, Jorgen S
van Hest, Jan C M
Rutjes, Floris P J T
author_sort Willemsen, Jorgen S
collection PubMed
description Water-soluble dendritic iridium catalysts were synthesized by attaching a reactive metal complex to DAB-Am dendrimers via an adapted asymmetric bipyridine ligand. These dendritic catalysts were applied in the aqueous reductive amination of valine while contained in a dialysis bag. Comparable conversions were observed as for the noncompartmentalized counterparts, albeit with somewhat longer reaction times. These results clearly show that the encapsulated catalyst system is suitable to successfully drive a complex reaction mixture with various equilibrium reactions to completion.
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spelling pubmed-36786152013-06-13 Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag Willemsen, Jorgen S van Hest, Jan C M Rutjes, Floris P J T Beilstein J Org Chem Full Research Paper Water-soluble dendritic iridium catalysts were synthesized by attaching a reactive metal complex to DAB-Am dendrimers via an adapted asymmetric bipyridine ligand. These dendritic catalysts were applied in the aqueous reductive amination of valine while contained in a dialysis bag. Comparable conversions were observed as for the noncompartmentalized counterparts, albeit with somewhat longer reaction times. These results clearly show that the encapsulated catalyst system is suitable to successfully drive a complex reaction mixture with various equilibrium reactions to completion. Beilstein-Institut 2013-05-17 /pmc/articles/PMC3678615/ /pubmed/23766812 http://dx.doi.org/10.3762/bjoc.9.110 Text en Copyright © 2013, Willemsen et al. https://creativecommons.org/licenses/by/2.0https://www.beilstein-journals.org/bjoc/termsThis is an Open Access article under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The license is subject to the Beilstein Journal of Organic Chemistry terms and conditions: (https://www.beilstein-journals.org/bjoc/terms)
spellingShingle Full Research Paper
Willemsen, Jorgen S
van Hest, Jan C M
Rutjes, Floris P J T
Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title_full Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title_fullStr Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title_full_unstemmed Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title_short Aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
title_sort aqueous reductive amination using a dendritic metal catalyst in a dialysis bag
topic Full Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3678615/
https://www.ncbi.nlm.nih.gov/pubmed/23766812
http://dx.doi.org/10.3762/bjoc.9.110
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