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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...

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Autores principales: Bielawski, Marcin, Malmgren, Joel, Pardo, Leticia M, Wikmark, Ylva, Olofsson, Berit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: WILEY-VCH Verlag 2014
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.
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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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