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Selective C–H Iodination of (Hetero)arenes
[Image: see text] Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we present a strategy for selective C–H iodination of (hetero)arenes with a broad functional group tolerance. We demonstrate the utility and differentiation to other iodination methods o...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289285/ https://www.ncbi.nlm.nih.gov/pubmed/34114468 http://dx.doi.org/10.1021/acs.orglett.1c01530 |
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author | Tanwar, Lalita Börgel, Jonas Lehmann, Johannes Ritter, Tobias |
author_facet | Tanwar, Lalita Börgel, Jonas Lehmann, Johannes Ritter, Tobias |
author_sort | Tanwar, Lalita |
collection | PubMed |
description | [Image: see text] Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we present a strategy for selective C–H iodination of (hetero)arenes with a broad functional group tolerance. We demonstrate the utility and differentiation to other iodination methods of supposed sulfonyl hypoiodites for a set of carboarenes and heteroarenes. |
format | Online Article Text |
id | pubmed-8289285 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-82892852021-07-20 Selective C–H Iodination of (Hetero)arenes Tanwar, Lalita Börgel, Jonas Lehmann, Johannes Ritter, Tobias Org Lett [Image: see text] Iodoarenes are versatile intermediates and common synthetic targets in organic synthesis. Here, we present a strategy for selective C–H iodination of (hetero)arenes with a broad functional group tolerance. We demonstrate the utility and differentiation to other iodination methods of supposed sulfonyl hypoiodites for a set of carboarenes and heteroarenes. American Chemical Society 2021-06-11 2021-07-02 /pmc/articles/PMC8289285/ /pubmed/34114468 http://dx.doi.org/10.1021/acs.orglett.1c01530 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Tanwar, Lalita Börgel, Jonas Lehmann, Johannes Ritter, Tobias Selective C–H Iodination of (Hetero)arenes |
title | Selective C–H Iodination of (Hetero)arenes |
title_full | Selective C–H Iodination of (Hetero)arenes |
title_fullStr | Selective C–H Iodination of (Hetero)arenes |
title_full_unstemmed | Selective C–H Iodination of (Hetero)arenes |
title_short | Selective C–H Iodination of (Hetero)arenes |
title_sort | selective c–h iodination of (hetero)arenes |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8289285/ https://www.ncbi.nlm.nih.gov/pubmed/34114468 http://dx.doi.org/10.1021/acs.orglett.1c01530 |
work_keys_str_mv | AT tanwarlalita selectivechiodinationofheteroarenes AT borgeljonas selectivechiodinationofheteroarenes AT lehmannjohannes selectivechiodinationofheteroarenes AT rittertobias selectivechiodinationofheteroarenes |