Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview

The last decade has witnessed the emergence of innovative synthetic tools for the synthesis of fluorinated molecules. Among these approaches, the transition-metal-catalyzed functionalization of various scaffolds with a panel of fluorinated groups (XRF, X = S, Se, O) offered straightforward access to...

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Main Authors: Louis Monsigny, Floriane Doche, Tatiana Besset
Format: Article
Language:English
Published: Beilstein-Institut 2023-04-01
Series:Beilstein Journal of Organic Chemistry
Subjects:
Online Access:https://doi.org/10.3762/bjoc.19.35
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author Louis Monsigny
Floriane Doche
Tatiana Besset
author_facet Louis Monsigny
Floriane Doche
Tatiana Besset
author_sort Louis Monsigny
collection DOAJ
description The last decade has witnessed the emergence of innovative synthetic tools for the synthesis of fluorinated molecules. Among these approaches, the transition-metal-catalyzed functionalization of various scaffolds with a panel of fluorinated groups (XRF, X = S, Se, O) offered straightforward access to high value-added compounds. This review will highlight the main advances made in the field with the transition-metal-catalyzed functionalization of C(sp2) and C(sp3) centers with SCF3, SeCF3, or OCH2CF3 groups among others, by C–H bond activation. The scope and limitations of these transformations are discussed in this review.
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spelling doaj.art-1d2c9624ac3e41789d000a15fcf3d1a42023-05-02T09:01:07ZengBeilstein-InstitutBeilstein Journal of Organic Chemistry1860-53972023-04-0119144847310.3762/bjoc.19.351860-5397-19-35Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overviewLouis Monsigny0Floriane Doche1Tatiana Besset2Normandie University, INSA Rouen, UNIROUEN, CNRS, COBRA (UMR 6014), 76000 Rouen, France Normandie University, INSA Rouen, UNIROUEN, CNRS, COBRA (UMR 6014), 76000 Rouen, France Normandie University, INSA Rouen, UNIROUEN, CNRS, COBRA (UMR 6014), 76000 Rouen, France The last decade has witnessed the emergence of innovative synthetic tools for the synthesis of fluorinated molecules. Among these approaches, the transition-metal-catalyzed functionalization of various scaffolds with a panel of fluorinated groups (XRF, X = S, Se, O) offered straightforward access to high value-added compounds. This review will highlight the main advances made in the field with the transition-metal-catalyzed functionalization of C(sp2) and C(sp3) centers with SCF3, SeCF3, or OCH2CF3 groups among others, by C–H bond activation. The scope and limitations of these transformations are discussed in this review.https://doi.org/10.3762/bjoc.19.35c–h bond activationemergent fluorinated groupshomogeneous catalysisorganofluorine chemistrypalladiumsynthetic method
spellingShingle Louis Monsigny
Floriane Doche
Tatiana Besset
Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
Beilstein Journal of Organic Chemistry
c–h bond activation
emergent fluorinated groups
homogeneous catalysis
organofluorine chemistry
palladium
synthetic method
title Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
title_full Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
title_fullStr Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
title_full_unstemmed Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
title_short Transition-metal-catalyzed C–H bond activation as a sustainable strategy for the synthesis of fluorinated molecules: an overview
title_sort transition metal catalyzed c h bond activation as a sustainable strategy for the synthesis of fluorinated molecules an overview
topic c–h bond activation
emergent fluorinated groups
homogeneous catalysis
organofluorine chemistry
palladium
synthetic method
url https://doi.org/10.3762/bjoc.19.35
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AT florianedoche transitionmetalcatalyzedchbondactivationasasustainablestrategyforthesynthesisoffluorinatedmoleculesanoverview
AT tatianabesset transitionmetalcatalyzedchbondactivationasasustainablestrategyforthesynthesisoffluorinatedmoleculesanoverview