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Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags
The effect of the presence of fluorous tags in bisoxazoline ligands on the stereoselectivity of the cobalt-catalyzed asymmetric Henry reaction was investigated. In contrast to the stereoselectivity obtained with conventional nonfluorous ligands, using bisoxazoline bidentate ligands featuring two flu...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675312/ https://www.ncbi.nlm.nih.gov/pubmed/38005354 http://dx.doi.org/10.3390/molecules28227632 |
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author | Ishihara, Kazuki Kato, Yamato Takeuchi, Narisa Hayashi, Yuka Hagiwara, Yuna Shibuya, Shyota Natsume, Tohya Matsugi, Masato |
author_facet | Ishihara, Kazuki Kato, Yamato Takeuchi, Narisa Hayashi, Yuka Hagiwara, Yuna Shibuya, Shyota Natsume, Tohya Matsugi, Masato |
author_sort | Ishihara, Kazuki |
collection | PubMed |
description | The effect of the presence of fluorous tags in bisoxazoline ligands on the stereoselectivity of the cobalt-catalyzed asymmetric Henry reaction was investigated. In contrast to the stereoselectivity obtained with conventional nonfluorous ligands, using bisoxazoline bidentate ligands featuring two fluorous tags in adjacent positions on the aromatic ring yielded a reversed stereoselectivity. The stereoselectivity also reversed when the fluorous tags were replaced with alkyl chains of equivalent length, albeit to a considerably lesser degree, highlighting the effect of the fluorous tags. |
format | Online Article Text |
id | pubmed-10675312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-106753122023-11-16 Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags Ishihara, Kazuki Kato, Yamato Takeuchi, Narisa Hayashi, Yuka Hagiwara, Yuna Shibuya, Shyota Natsume, Tohya Matsugi, Masato Molecules Article The effect of the presence of fluorous tags in bisoxazoline ligands on the stereoselectivity of the cobalt-catalyzed asymmetric Henry reaction was investigated. In contrast to the stereoselectivity obtained with conventional nonfluorous ligands, using bisoxazoline bidentate ligands featuring two fluorous tags in adjacent positions on the aromatic ring yielded a reversed stereoselectivity. The stereoselectivity also reversed when the fluorous tags were replaced with alkyl chains of equivalent length, albeit to a considerably lesser degree, highlighting the effect of the fluorous tags. MDPI 2023-11-16 /pmc/articles/PMC10675312/ /pubmed/38005354 http://dx.doi.org/10.3390/molecules28227632 Text en © 2023 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 | Article Ishihara, Kazuki Kato, Yamato Takeuchi, Narisa Hayashi, Yuka Hagiwara, Yuna Shibuya, Shyota Natsume, Tohya Matsugi, Masato Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title | Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title_full | Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title_fullStr | Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title_full_unstemmed | Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title_short | Asymmetric Henry Reaction Using Cobalt Complexes with Bisoxazoline Ligands Bearing Two Fluorous Tags |
title_sort | asymmetric henry reaction using cobalt complexes with bisoxazoline ligands bearing two fluorous tags |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10675312/ https://www.ncbi.nlm.nih.gov/pubmed/38005354 http://dx.doi.org/10.3390/molecules28227632 |
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