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A one-pot cascade protocol for diarylation of amines and water
N- and O-arylated compounds are prevalent in pharmaceuticals and materials, and efficient approaches for their synthesis are important. Herein, we present an efficient protocol for the diarylation of aliphatic amines and water with two structurally different aryl groups in one single step, yielding...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519595/ https://www.ncbi.nlm.nih.gov/pubmed/36149800 http://dx.doi.org/10.1016/j.xpro.2022.101700 |
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author | Linde, Erika Olofsson, Berit |
author_facet | Linde, Erika Olofsson, Berit |
author_sort | Linde, Erika |
collection | PubMed |
description | N- and O-arylated compounds are prevalent in pharmaceuticals and materials, and efficient approaches for their synthesis are important. Herein, we present an efficient protocol for the diarylation of aliphatic amines and water with two structurally different aryl groups in one single step, yielding highly functionalized diaryl amines and ethers. We describe the synthesis of the required diaryliodonium salts and detail the procedure for the diarylation. The protocol is limited to use of unhindered amines and diaryliodonium salts with certain substituents. For complete details on the use and execution of this protocol, please refer to Linde et al. (2022). |
format | Online Article Text |
id | pubmed-9519595 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-95195952022-09-30 A one-pot cascade protocol for diarylation of amines and water Linde, Erika Olofsson, Berit STAR Protoc Protocol N- and O-arylated compounds are prevalent in pharmaceuticals and materials, and efficient approaches for their synthesis are important. Herein, we present an efficient protocol for the diarylation of aliphatic amines and water with two structurally different aryl groups in one single step, yielding highly functionalized diaryl amines and ethers. We describe the synthesis of the required diaryliodonium salts and detail the procedure for the diarylation. The protocol is limited to use of unhindered amines and diaryliodonium salts with certain substituents. For complete details on the use and execution of this protocol, please refer to Linde et al. (2022). Elsevier 2022-09-22 /pmc/articles/PMC9519595/ /pubmed/36149800 http://dx.doi.org/10.1016/j.xpro.2022.101700 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Protocol Linde, Erika Olofsson, Berit A one-pot cascade protocol for diarylation of amines and water |
title | A one-pot cascade protocol for diarylation of amines and water |
title_full | A one-pot cascade protocol for diarylation of amines and water |
title_fullStr | A one-pot cascade protocol for diarylation of amines and water |
title_full_unstemmed | A one-pot cascade protocol for diarylation of amines and water |
title_short | A one-pot cascade protocol for diarylation of amines and water |
title_sort | one-pot cascade protocol for diarylation of amines and water |
topic | Protocol |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9519595/ https://www.ncbi.nlm.nih.gov/pubmed/36149800 http://dx.doi.org/10.1016/j.xpro.2022.101700 |
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