The incorporation of fluoroalkyl groups, and particularly the trifluoromethyl group, in pharmaceutical molecules has a profound impact on their physical and biological properties, mainly because of the unique metabolic ...

Perfluorobutylation of a series of benzo- and dibenzo-(hetero)aromatic compounds without formal leaving groups is achieved efficiently in organic solvent: water mixtures under photostimulation. The methodology is compared ...

In this work, we present a room- or solar-light-initiated transition-metal-free radical homolytic aromatic substitution (HAS) reaction of aniline derivatives with perfluoroalkyl moieties employing perfluoroalkyl halides ...

Perfluorobutylation of a series of benzo(hetero)aromatic compounds without formal leaving groups is achieved efficaciously in organic solvent-water mixtures under photostimulation. The methodology is compared with previously ...

Perfluorobutylation of a series of benzo- and dibenzo-(hetero)aromatic compounds without formal leaving groups is achieved efficiently in organic solvent: water mixtures under photostimulation. The methodology is compared ...

Radical initiation for the perfluoroalkylation reaction of amino(hetero)aromatics has been accomplishedemploying the complex [(TMEDA)I$I3] and visible light. This methodology circumvents the use ofmetal(organo)catalysts ...

Perfluoroalkylation reactions of arenes have not been the subject of intense study as has been the case for the trifluoromethylation reactions of aromatics. However, the new synthetic methods proposed for achieving homolytic ...

Fluoroalkylation reactions of (hetero)aromatics have been accomplished through the low-power illumination from red LEDs (λ max = 635 nm) of commercially available perfluoroalkyl iodides R F -I and phthalocyanine zinc salt ...

The photoinduced electron transfer (PET) substitution reaction of electron-rich aromatic nuclei with perfluoroalkyl Rf groups was carried out in water or aqueous mixtures to render substitution products resulting from ...

Electron-donor-acceptor complexes (EDA) can be established through halogen-bonding interactions between the N lone electron pair from organic bases (or N-/O-centered anions) and perfluoroalkyl iodides RF–I. These EDA ...