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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...

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Detalles Bibliográficos
Autores principales: Wang, Dong, Carlton, C. Grace, Tayu, Masanori, McDouall, Joseph J. W., Perry, Gregory J. P., Procter, David J.
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/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.
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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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