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One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts
An efficient one-pot synthesis of N-heteroaryl iodonium triflates from the corresponding N-heteroaryl iodide and arene has been developed. The reaction conditions resemble our previous one-pot syntheses, with suitable modifications to allow N-heteroaryl groups. The reaction time is only 30 min, and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
WILEY-VCH Verlag
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943608/ https://www.ncbi.nlm.nih.gov/pubmed/24688890 http://dx.doi.org/10.1002/open.201300042 |
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author | Bielawski, Marcin Malmgren, Joel Pardo, Leticia M Wikmark, Ylva Olofsson, Berit |
author_facet | Bielawski, Marcin Malmgren, Joel Pardo, Leticia M Wikmark, Ylva Olofsson, Berit |
author_sort | Bielawski, Marcin |
collection | PubMed |
description | An efficient one-pot synthesis of N-heteroaryl iodonium triflates from the corresponding N-heteroaryl iodide and arene has been developed. The reaction conditions resemble our previous one-pot syntheses, with suitable modifications to allow N-heteroaryl groups. The reaction time is only 30 min, and no anion exchange is required. The obtained iodonium salts were isolated in a protonated form, these salts can either be employed directly in applications or be deprotonated prior to use. The aryl groups were chosen to induce chemoselective transfer of the heteroaryl moiety to various nucleophiles. The reactivity and chemoselectivity of these iodonium salts were demonstrated by selectively introducing a pyridyl moiety onto both oxygen and carbon nucleophiles in good yields. |
format | Online Article Text |
id | pubmed-3943608 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | WILEY-VCH Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-39436082014-03-31 One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts Bielawski, Marcin Malmgren, Joel Pardo, Leticia M Wikmark, Ylva Olofsson, Berit ChemistryOpen Communications An efficient one-pot synthesis of N-heteroaryl iodonium triflates from the corresponding N-heteroaryl iodide and arene has been developed. The reaction conditions resemble our previous one-pot syntheses, with suitable modifications to allow N-heteroaryl groups. The reaction time is only 30 min, and no anion exchange is required. The obtained iodonium salts were isolated in a protonated form, these salts can either be employed directly in applications or be deprotonated prior to use. The aryl groups were chosen to induce chemoselective transfer of the heteroaryl moiety to various nucleophiles. The reactivity and chemoselectivity of these iodonium salts were demonstrated by selectively introducing a pyridyl moiety onto both oxygen and carbon nucleophiles in good yields. WILEY-VCH Verlag 2014-02 2014-01-23 /pmc/articles/PMC3943608/ /pubmed/24688890 http://dx.doi.org/10.1002/open.201300042 Text en © 2014 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. http://creativecommons.org/licenses/by/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial 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 Bielawski, Marcin Malmgren, Joel Pardo, Leticia M Wikmark, Ylva Olofsson, Berit One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title | One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title_full | One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title_fullStr | One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title_full_unstemmed | One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title_short | One-Pot Synthesis and Applications of N-Heteroaryl Iodonium Salts |
title_sort | one-pot synthesis and applications of n-heteroaryl iodonium salts |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3943608/ https://www.ncbi.nlm.nih.gov/pubmed/24688890 http://dx.doi.org/10.1002/open.201300042 |
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