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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...

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Autores principales: Wonner, Patrick, Dreger, Alexander, Vogel, Lukas, Engelage, Elric, Huber, Stefan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
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.
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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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