Fluorinated radicals in water are shown to enable a useful array of synthetic organic transformations, reflecting these intermediates' distinct behavior in water or aqueous media. The enhanced reactivities of perfluroalkyl radicals in water facilitate their addition reactions to carbon–carbon and carbon–heteroatom multiple bonds. Activated and unactivated unsaturated substrates are equally reactive candidates for radical perfluoroalkylation reactions in aqueous systems. Parallel behavior of perfluorinated radicals in organic solvents and in water is presented, demonstrating the scope of reactions based on fluorinated radicals in aqueous media, as well as the ease of carbocyclic construction.Fil: Barata Vallejo, Sebastian. Universidad de Bue...
New reagents for selective radical fluorine transfer have been identified and utilized to develop tw...
none5noThe reactions of alkylperoxyl radicals with phenols have remained difficult to investigate in...
Perfluorobutylation of a series of benzo(hetero)aromatic compounds without formal leaving groups is ...
Figure presented. Perfluoroalkyl-substituted compounds are regarded as important components of fluor...
This account is focused on carbon-carbon, and carbon-sulphur bond-forming reactions through the use ...
Recent protocols and reactions for catalytic radical perfluoroalkylations will be described. The pro...
The radical or radical ion-based fluorination reactions of organic compounds will be presented. Thes...
Several organic radical transformations in aqueous media using organometallic chemistry are presente...
This account is focused on highlighting the recent advances on synthetically-useful organic reaction...
The selective fluorination of organic molecules has become increasingly important for the pharmaceut...
The generation of perfluoroalkyl radicals (RF) by means of photocatalysis is a more suitable route t...
The photoinduced electron transfer (PET) substitution reaction of electron-rich aromatic nuclei with...
Radical anions are formed on addition of hydrated electrons to pentafluoroacetophenone (PFA) and pen...
Hydroperfluorobutylation of a series of electron-deficient and electron-rich alkenes through consecu...
Perfluorobutylation of a series of benzo- and dibenzo-(hetero)aromatic compounds without formal lea...
New reagents for selective radical fluorine transfer have been identified and utilized to develop tw...
none5noThe reactions of alkylperoxyl radicals with phenols have remained difficult to investigate in...
Perfluorobutylation of a series of benzo(hetero)aromatic compounds without formal leaving groups is ...
Figure presented. Perfluoroalkyl-substituted compounds are regarded as important components of fluor...
This account is focused on carbon-carbon, and carbon-sulphur bond-forming reactions through the use ...
Recent protocols and reactions for catalytic radical perfluoroalkylations will be described. The pro...
The radical or radical ion-based fluorination reactions of organic compounds will be presented. Thes...
Several organic radical transformations in aqueous media using organometallic chemistry are presente...
This account is focused on highlighting the recent advances on synthetically-useful organic reaction...
The selective fluorination of organic molecules has become increasingly important for the pharmaceut...
The generation of perfluoroalkyl radicals (RF) by means of photocatalysis is a more suitable route t...
The photoinduced electron transfer (PET) substitution reaction of electron-rich aromatic nuclei with...
Radical anions are formed on addition of hydrated electrons to pentafluoroacetophenone (PFA) and pen...
Hydroperfluorobutylation of a series of electron-deficient and electron-rich alkenes through consecu...
Perfluorobutylation of a series of benzo- and dibenzo-(hetero)aromatic compounds without formal lea...
New reagents for selective radical fluorine transfer have been identified and utilized to develop tw...
none5noThe reactions of alkylperoxyl radicals with phenols have remained difficult to investigate in...
Perfluorobutylation of a series of benzo(hetero)aromatic compounds without formal leaving groups is ...