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Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction
Chalcogen bonding is the non‐covalent interaction between Lewis acidic chalcogen substituents and Lewis bases. Herein, we present the first application of dicationic tellurium‐based chalcogen bond donors in the nitro‐Michael reaction between trans‐β‐nitrostyrene and indoles. This also constitutes th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899570/ https://www.ncbi.nlm.nih.gov/pubmed/31535789 http://dx.doi.org/10.1002/anie.201910639 |
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author | Wonner, Patrick Dreger, Alexander Vogel, Lukas Engelage, Elric Huber, Stefan M. |
author_facet | Wonner, Patrick Dreger, Alexander Vogel, Lukas Engelage, Elric Huber, Stefan M. |
author_sort | Wonner, Patrick |
collection | PubMed |
description | Chalcogen bonding is the non‐covalent interaction between Lewis acidic chalcogen substituents and Lewis bases. Herein, we present the first application of dicationic tellurium‐based chalcogen bond donors in the nitro‐Michael reaction between trans‐β‐nitrostyrene and indoles. This also constitutes the first activation of nitro derivatives by chalcogen bonding (and halogen bonding). The catalysts showed rate accelerations of more than a factor of 300 compared to strongly Lewis acidic hydrogen bond donors. Several comparison experiments, titrations, and DFT calculations support a chalcogen‐bonding‐based mode of activation of β‐nitrostyrene. |
format | Online Article Text |
id | pubmed-6899570 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68995702019-12-19 Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction Wonner, Patrick Dreger, Alexander Vogel, Lukas Engelage, Elric Huber, Stefan M. Angew Chem Int Ed Engl Communications Chalcogen bonding is the non‐covalent interaction between Lewis acidic chalcogen substituents and Lewis bases. Herein, we present the first application of dicationic tellurium‐based chalcogen bond donors in the nitro‐Michael reaction between trans‐β‐nitrostyrene and indoles. This also constitutes the first activation of nitro derivatives by chalcogen bonding (and halogen bonding). The catalysts showed rate accelerations of more than a factor of 300 compared to strongly Lewis acidic hydrogen bond donors. Several comparison experiments, titrations, and DFT calculations support a chalcogen‐bonding‐based mode of activation of β‐nitrostyrene. John Wiley and Sons Inc. 2019-10-23 2019-11-18 /pmc/articles/PMC6899570/ /pubmed/31535789 http://dx.doi.org/10.1002/anie.201910639 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Wonner, Patrick Dreger, Alexander Vogel, Lukas Engelage, Elric Huber, Stefan M. Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title | Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title_full | Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title_fullStr | Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title_full_unstemmed | Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title_short | Chalcogen Bonding Catalysis of a Nitro‐Michael Reaction |
title_sort | chalcogen bonding catalysis of a nitro‐michael reaction |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6899570/ https://www.ncbi.nlm.nih.gov/pubmed/31535789 http://dx.doi.org/10.1002/anie.201910639 |
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