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Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts
Asymmetric transfer hydrogenation (ATH) is an important process in organic synthesis for which the Noyori‐type Ru(II) catalysts [(arene)Ru(Tsdiamine)] are now well established and widely used. We now demonstrate for the first time the catalytic activity of the osmium analogues. X‐ray crystal structu...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY‐VCH Verlag
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832837/ https://www.ncbi.nlm.nih.gov/pubmed/25853228 http://dx.doi.org/10.1002/chem.201500534 |
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author | Coverdale, James P. C. Sanchez‐Cano, Carlos Clarkson, Guy J. Soni, Rina Wills, Martin Sadler, Peter J. |
author_facet | Coverdale, James P. C. Sanchez‐Cano, Carlos Clarkson, Guy J. Soni, Rina Wills, Martin Sadler, Peter J. |
author_sort | Coverdale, James P. C. |
collection | PubMed |
description | Asymmetric transfer hydrogenation (ATH) is an important process in organic synthesis for which the Noyori‐type Ru(II) catalysts [(arene)Ru(Tsdiamine)] are now well established and widely used. We now demonstrate for the first time the catalytic activity of the osmium analogues. X‐ray crystal structures of the 16‐electron Os(II) catalysts are almost identical to those of Ru(II). Intriguingly the precursor complex was isolated as a dichlorido complex with a monodentate amine ligand. The Os(II) catalysts are readily synthesised (within 1 h) and exhibit excellent enantioselectivity in ATH reactions of ketones. |
format | Online Article Text |
id | pubmed-4832837 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | WILEY‐VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-48328372016-04-27 Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts Coverdale, James P. C. Sanchez‐Cano, Carlos Clarkson, Guy J. Soni, Rina Wills, Martin Sadler, Peter J. Chemistry Communications Asymmetric transfer hydrogenation (ATH) is an important process in organic synthesis for which the Noyori‐type Ru(II) catalysts [(arene)Ru(Tsdiamine)] are now well established and widely used. We now demonstrate for the first time the catalytic activity of the osmium analogues. X‐ray crystal structures of the 16‐electron Os(II) catalysts are almost identical to those of Ru(II). Intriguingly the precursor complex was isolated as a dichlorido complex with a monodentate amine ligand. The Os(II) catalysts are readily synthesised (within 1 h) and exhibit excellent enantioselectivity in ATH reactions of ketones. WILEY‐VCH Verlag 2015-04-08 2015-05-26 /pmc/articles/PMC4832837/ /pubmed/25853228 http://dx.doi.org/10.1002/chem.201500534 Text en © 2015 The Authors. Published by Wiley‐VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. Open access. |
spellingShingle | Communications Coverdale, James P. C. Sanchez‐Cano, Carlos Clarkson, Guy J. Soni, Rina Wills, Martin Sadler, Peter J. Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title | Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title_full | Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title_fullStr | Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title_full_unstemmed | Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title_short | Easy To Synthesize, Robust Organo‐osmium Asymmetric Transfer Hydrogenation Catalysts |
title_sort | easy to synthesize, robust organo‐osmium asymmetric transfer hydrogenation catalysts |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4832837/ https://www.ncbi.nlm.nih.gov/pubmed/25853228 http://dx.doi.org/10.1002/chem.201500534 |
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