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Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation
Trifluoromethyl sulfoxides are a new class of trifluoromethylthiolating reagent. The sulfoxides engage in metal‐free C−H trifluoromethylthiolation with a range of (hetero)arenes. The method is also applicable to the functionalization of important compound classes, such as ligand derivatives and poly...
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/PMC7540508/ https://www.ncbi.nlm.nih.gov/pubmed/32463942 http://dx.doi.org/10.1002/anie.202005531 |
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author | Wang, Dong Carlton, C. Grace Tayu, Masanori McDouall, Joseph J. W. Perry, Gregory J. P. Procter, David J. |
author_facet | Wang, Dong Carlton, C. Grace Tayu, Masanori McDouall, Joseph J. W. Perry, Gregory J. P. Procter, David J. |
author_sort | Wang, Dong |
collection | PubMed |
description | Trifluoromethyl sulfoxides are a new class of trifluoromethylthiolating reagent. The sulfoxides engage in metal‐free C−H trifluoromethylthiolation with a range of (hetero)arenes. The method is also applicable to the functionalization of important compound classes, such as ligand derivatives and polyaromatics, and in the late‐stage trifluoromethylthiolation of medicines and agrochemicals. The isolation and characterization of a sulfonium salt intermediate supports an interrupted Pummerer reaction mechanism. |
format | Online Article Text |
id | pubmed-7540508 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75405082020-10-09 Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation Wang, Dong Carlton, C. Grace Tayu, Masanori McDouall, Joseph J. W. Perry, Gregory J. P. Procter, David J. Angew Chem Int Ed Engl Communications Trifluoromethyl sulfoxides are a new class of trifluoromethylthiolating reagent. The sulfoxides engage in metal‐free C−H trifluoromethylthiolation with a range of (hetero)arenes. The method is also applicable to the functionalization of important compound classes, such as ligand derivatives and polyaromatics, and in the late‐stage trifluoromethylthiolation of medicines and agrochemicals. The isolation and characterization of a sulfonium salt intermediate supports an interrupted Pummerer reaction mechanism. John Wiley and Sons Inc. 2020-07-15 2020-09-07 /pmc/articles/PMC7540508/ /pubmed/32463942 http://dx.doi.org/10.1002/anie.202005531 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, Dong Carlton, C. Grace Tayu, Masanori McDouall, Joseph J. W. Perry, Gregory J. P. Procter, David J. Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title | Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title_full | Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title_fullStr | Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title_full_unstemmed | Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title_short | Trifluoromethyl Sulfoxides: Reagents for Metal‐Free C−H Trifluoromethylthiolation |
title_sort | trifluoromethyl sulfoxides: reagents for metal‐free c−h trifluoromethylthiolation |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7540508/ https://www.ncbi.nlm.nih.gov/pubmed/32463942 http://dx.doi.org/10.1002/anie.202005531 |
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