6533b862fe1ef96bd12c6dd8
RESEARCH PRODUCT
Palladium‐Catalyzed Electrophilic C–H‐Bond Fluorination: Mechanistic Overview and Supporting Evidence
Julien RogerJean-cyrille HiersoJean-cyrille HiersoChristelle TestaPaul Fleurat-lessardsubject
Reaction mechanismC h bond[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryReaction mechanismsOrganic Chemistrychemistry.chemical_element[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistry01 natural sciencesMedicinal chemistryCatalysis Fluorination0104 chemical sciencesCatalysisC–H halogenationElectrophilePhysical and Theoretical ChemistryFluorinated compoundsPalladiumPalladiumdescription
International audience; Palladium-catalyzed electrophilic fluorination is a particularly attractive and challenging synthetic issue. Because of the rapid evolution of this topic, a critical point on the mechanistic and experimental advances is provided herein. In the present review, we focused on current mechanistic understanding in electrophilic fluorination (and related halogenations) catalyzed by palladium, mainly with N-directing group. Our discussion is based on the well-characterized or calculated pertinent metal species and intermediates used for analyzing the plausible catalytic cycles. A particular effort has been devoted to gathering supporting data for the putative species involved in catalysis, such as mass data, NMR in solution (19F, 31P) and X-ray structures, often supported by theoretical approaches. The cut-off of this review is March 2018.
year | journal | country | edition | language |
---|---|---|---|---|
2018-11-25 | European Journal of Organic Chemistry |