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Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone
A straightforward synthesis of diaryliodonium salts is achieved by using Oxone as the stoichiometric oxidant. Slow addition is the key to obtaining good yields and purities of the reaction products, which are highly useful reagents in many different areas of organic synthesis.
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288754/ https://www.ncbi.nlm.nih.gov/pubmed/28168145 http://dx.doi.org/10.1002/open.201600129 |
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author | Soldatova, Natalia Postnikov, Pavel Kukurina, Olga Zhdankin, Viktor V. Yoshimura, Akira Wirth, Thomas Yusubov, Mekhman S. |
author_facet | Soldatova, Natalia Postnikov, Pavel Kukurina, Olga Zhdankin, Viktor V. Yoshimura, Akira Wirth, Thomas Yusubov, Mekhman S. |
author_sort | Soldatova, Natalia |
collection | PubMed |
description | A straightforward synthesis of diaryliodonium salts is achieved by using Oxone as the stoichiometric oxidant. Slow addition is the key to obtaining good yields and purities of the reaction products, which are highly useful reagents in many different areas of organic synthesis. |
format | Online Article Text |
id | pubmed-5288754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52887542017-02-06 Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone Soldatova, Natalia Postnikov, Pavel Kukurina, Olga Zhdankin, Viktor V. Yoshimura, Akira Wirth, Thomas Yusubov, Mekhman S. ChemistryOpen Communications A straightforward synthesis of diaryliodonium salts is achieved by using Oxone as the stoichiometric oxidant. Slow addition is the key to obtaining good yields and purities of the reaction products, which are highly useful reagents in many different areas of organic synthesis. John Wiley and Sons Inc. 2016-12-16 /pmc/articles/PMC5288754/ /pubmed/28168145 http://dx.doi.org/10.1002/open.201600129 Text en © 2016 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://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 | Communications Soldatova, Natalia Postnikov, Pavel Kukurina, Olga Zhdankin, Viktor V. Yoshimura, Akira Wirth, Thomas Yusubov, Mekhman S. Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title | Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title_full | Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title_fullStr | Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title_full_unstemmed | Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title_short | Facile One‐Pot Synthesis of Diaryliodonium Salts from Arenes and Aryl Iodides with Oxone |
title_sort | facile one‐pot synthesis of diaryliodonium salts from arenes and aryl iodides with oxone |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5288754/ https://www.ncbi.nlm.nih.gov/pubmed/28168145 http://dx.doi.org/10.1002/open.201600129 |
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