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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8271416 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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