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Photocatalytic Fluoro Sulfoximidations of Styrenes
Reactions of difluoroiodotoluene with NH‐sulfoximines provide new hypervalent iodine(III) reagents, which photocatalytically transfer a fluoro and a sulfoximidoyl group onto styrenes with high regioselectivity. The substrate scope is broad with respect to both sulfoximines and olefins. Following an...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496861/ https://www.ncbi.nlm.nih.gov/pubmed/32415689 http://dx.doi.org/10.1002/anie.202005844 |
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author | Wang, Chenyang Tu, Yongliang Ma, Ding Bolm, Carsten |
author_facet | Wang, Chenyang Tu, Yongliang Ma, Ding Bolm, Carsten |
author_sort | Wang, Chenyang |
collection | PubMed |
description | Reactions of difluoroiodotoluene with NH‐sulfoximines provide new hypervalent iodine(III) reagents, which photocatalytically transfer a fluoro and a sulfoximidoyl group onto styrenes with high regioselectivity. The substrate scope is broad with respect to both sulfoximines and olefins. Following an operationally simple protocol, a large library of fluorine‐containing N‐functionalized sulfoximines can be accessed. Results from mechanistic investigations revealed the importance of radical intermediates. |
format | Online Article Text |
id | pubmed-7496861 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-74968612020-09-25 Photocatalytic Fluoro Sulfoximidations of Styrenes Wang, Chenyang Tu, Yongliang Ma, Ding Bolm, Carsten Angew Chem Int Ed Engl Communications Reactions of difluoroiodotoluene with NH‐sulfoximines provide new hypervalent iodine(III) reagents, which photocatalytically transfer a fluoro and a sulfoximidoyl group onto styrenes with high regioselectivity. The substrate scope is broad with respect to both sulfoximines and olefins. Following an operationally simple protocol, a large library of fluorine‐containing N‐functionalized sulfoximines can be accessed. Results from mechanistic investigations revealed the importance of radical intermediates. John Wiley and Sons Inc. 2020-06-08 2020-08-10 /pmc/articles/PMC7496861/ /pubmed/32415689 http://dx.doi.org/10.1002/anie.202005844 Text en © 2020 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Communications Wang, Chenyang Tu, Yongliang Ma, Ding Bolm, Carsten Photocatalytic Fluoro Sulfoximidations of Styrenes |
title | Photocatalytic Fluoro Sulfoximidations of Styrenes |
title_full | Photocatalytic Fluoro Sulfoximidations of Styrenes |
title_fullStr | Photocatalytic Fluoro Sulfoximidations of Styrenes |
title_full_unstemmed | Photocatalytic Fluoro Sulfoximidations of Styrenes |
title_short | Photocatalytic Fluoro Sulfoximidations of Styrenes |
title_sort | photocatalytic fluoro sulfoximidations of styrenes |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7496861/ https://www.ncbi.nlm.nih.gov/pubmed/32415689 http://dx.doi.org/10.1002/anie.202005844 |
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