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New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes
Gold(I) catalysts are ideal for the activation of alkynes under very mild conditions. However, unlike allenes or alkenes, the triple bond of alkynes cannot be prochiral. In addition, the linear coordination displayed by gold(I) complexes places the chiral ligand far away from the substrate resulting...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457203/ https://www.ncbi.nlm.nih.gov/pubmed/34472729 http://dx.doi.org/10.1002/cplu.202100232 |
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author | Zuccarello, Giuseppe Escofet, Imma Caniparoli, Ulysse Echavarren, Antonio M. |
author_facet | Zuccarello, Giuseppe Escofet, Imma Caniparoli, Ulysse Echavarren, Antonio M. |
author_sort | Zuccarello, Giuseppe |
collection | PubMed |
description | Gold(I) catalysts are ideal for the activation of alkynes under very mild conditions. However, unlike allenes or alkenes, the triple bond of alkynes cannot be prochiral. In addition, the linear coordination displayed by gold(I) complexes places the chiral ligand far away from the substrate resulting in an inefficient transfer of chiral information. This poses a significant challenge for the achievement of high enantiocontrol in gold(I)‐catalyzed reactions of alkynes. Although considerable progress on enantioselective gold(I)‐catalyzed transformations has recently been achieved, the asymmetric activation of non‐prochiral alkyne‐containing small molecules still represents a great challenge. Herein we summarize recent advances in intra‐ and intermolecular enantioselective gold(I)‐catalyzed reactions involving alkynes, discussing new chiral ligand designs that lie at the basis of these developments. We also focus on the mode of action of these catalysts, their possible limitations towards a next‐generation of more efficient ligand designs. Finally, square planar chiral gold(III) complexes, which offer an alternative to chiral gold(I) complexes, are also discussed. |
format | Online Article Text |
id | pubmed-8457203 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-84572032021-09-28 New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes Zuccarello, Giuseppe Escofet, Imma Caniparoli, Ulysse Echavarren, Antonio M. Chempluschem Minireviews Gold(I) catalysts are ideal for the activation of alkynes under very mild conditions. However, unlike allenes or alkenes, the triple bond of alkynes cannot be prochiral. In addition, the linear coordination displayed by gold(I) complexes places the chiral ligand far away from the substrate resulting in an inefficient transfer of chiral information. This poses a significant challenge for the achievement of high enantiocontrol in gold(I)‐catalyzed reactions of alkynes. Although considerable progress on enantioselective gold(I)‐catalyzed transformations has recently been achieved, the asymmetric activation of non‐prochiral alkyne‐containing small molecules still represents a great challenge. Herein we summarize recent advances in intra‐ and intermolecular enantioselective gold(I)‐catalyzed reactions involving alkynes, discussing new chiral ligand designs that lie at the basis of these developments. We also focus on the mode of action of these catalysts, their possible limitations towards a next‐generation of more efficient ligand designs. Finally, square planar chiral gold(III) complexes, which offer an alternative to chiral gold(I) complexes, are also discussed. John Wiley and Sons Inc. 2021-09-02 2021-09 /pmc/articles/PMC8457203/ /pubmed/34472729 http://dx.doi.org/10.1002/cplu.202100232 Text en © 2021 The Authors. ChemPlusChem published by Wiley-VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Minireviews Zuccarello, Giuseppe Escofet, Imma Caniparoli, Ulysse Echavarren, Antonio M. New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title | New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title_full | New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title_fullStr | New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title_full_unstemmed | New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title_short | New‐Generation Ligand Design for the Gold‐Catalyzed Asymmetric Activation of Alkynes |
title_sort | new‐generation ligand design for the gold‐catalyzed asymmetric activation of alkynes |
topic | Minireviews |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8457203/ https://www.ncbi.nlm.nih.gov/pubmed/34472729 http://dx.doi.org/10.1002/cplu.202100232 |
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