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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...

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Detalles Bibliográficos
Autores principales: Wang, Chenyang, Tu, Yongliang, Ma, Ding, Bolm, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
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.
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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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