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Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts

In this review, we describe the synthesis and use in hydrogen transfer reactions of ruthenacycles and iridacycles. The review limits itself to metallacycles where a ligand is bound in bidentate fashion to either ruthenium or iridium via a carbon–metal sigma bond, as well as a dative bond from a hete...

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Autores principales: Ritleng, Vincent, de Vries, Johannes G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271416/
https://www.ncbi.nlm.nih.gov/pubmed/34279416
http://dx.doi.org/10.3390/molecules26134076
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author Ritleng, Vincent
de Vries, Johannes G.
author_facet Ritleng, Vincent
de Vries, Johannes G.
author_sort Ritleng, Vincent
collection PubMed
description In this review, we describe the synthesis and use in hydrogen transfer reactions of ruthenacycles and iridacycles. The review limits itself to metallacycles where a ligand is bound in bidentate fashion to either ruthenium or iridium via a carbon–metal sigma bond, as well as a dative bond from a heteroatom or an N-heterocyclic carbene. Pincer complexes fall outside the scope. Described are applications in (asymmetric) transfer hydrogenation of aldehydes, ketones, and imines, as well as reductive aminations. Oxidation reactions, i.e., classical Oppenauer oxidation, which is the reverse of transfer hydrogenation, as well as dehydrogenations and oxidations with oxygen, are described. Racemizations of alcohols and secondary amines are also catalyzed by ruthenacycles and iridacycles.
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spelling pubmed-82714162021-07-11 Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts Ritleng, Vincent de Vries, Johannes G. Molecules Review In this review, we describe the synthesis and use in hydrogen transfer reactions of ruthenacycles and iridacycles. The review limits itself to metallacycles where a ligand is bound in bidentate fashion to either ruthenium or iridium via a carbon–metal sigma bond, as well as a dative bond from a heteroatom or an N-heterocyclic carbene. Pincer complexes fall outside the scope. Described are applications in (asymmetric) transfer hydrogenation of aldehydes, ketones, and imines, as well as reductive aminations. Oxidation reactions, i.e., classical Oppenauer oxidation, which is the reverse of transfer hydrogenation, as well as dehydrogenations and oxidations with oxygen, are described. Racemizations of alcohols and secondary amines are also catalyzed by ruthenacycles and iridacycles. MDPI 2021-07-03 /pmc/articles/PMC8271416/ /pubmed/34279416 http://dx.doi.org/10.3390/molecules26134076 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Ritleng, Vincent
de Vries, Johannes G.
Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title_full Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title_fullStr Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title_full_unstemmed Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title_short Ruthenacycles and Iridacycles as Transfer Hydrogenation Catalysts
title_sort ruthenacycles and iridacycles as transfer hydrogenation catalysts
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8271416/
https://www.ncbi.nlm.nih.gov/pubmed/34279416
http://dx.doi.org/10.3390/molecules26134076
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