Efficient syntheses of 3,3-difluorooxindoles and 3-fluorooxindoles via fluorination of hydrazonoindolin-2-one with Selectfluor are reported. Under different solvent conditions, this method produced 3,3-difluorooxindoles and 3-fluorooxindoles selectively. The broad substrate scope and mild reaction conditions make this transformation a valuable method in drug discovery and development
A practical synthesis of α-fluorinated imides via the catalyst-free fluorohydroxylation of ynamides ...
3,3-Difluoro-2-oxindoles can be obtained directly from indoles in moderate yields <i>via</i> electro...
Organofluorine substrates are molecules of increasing demand in both academic and industrial setting...
Fluorination of trialkylstannylindoles with caesium fluoroxysulfate or Selectfluor(TM) was investiga...
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic f...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Structurally diverse ketones, 1,3-diketones, and β-ketoesters, were selectively monofluorinated with...
The fluorination of 3-acetyl-2-oxindole with N-fluorobenzenesulfonimide under Lewis acid catalysis u...
fluorinated building blocks; fluoroarylacetic acid; fluoromalonate; fluorooxindole; organo-fluorine;...
An efficient difluorohydroxylation of substituted indoles leading to 3,3-difluoroindolin-2-ols with ...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
Fluorine chemistry plays a diverse role in the pharmaceutical, agricultural, and material industries...
Organofluorine compounds exhibit biological activity and have advantageous properties for drug desig...
Many pharmaceuticals have fused ring systems and their bioactivity tends to increase with the introd...
2015-07-17This dissertation mainly explored two aspects in organofluorine chemistry, the development...
A practical synthesis of α-fluorinated imides via the catalyst-free fluorohydroxylation of ynamides ...
3,3-Difluoro-2-oxindoles can be obtained directly from indoles in moderate yields <i>via</i> electro...
Organofluorine substrates are molecules of increasing demand in both academic and industrial setting...
Fluorination of trialkylstannylindoles with caesium fluoroxysulfate or Selectfluor(TM) was investiga...
A convenient and metal/catalyst-free approach for the reversal of regioselectivity in nucleophilic f...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Structurally diverse ketones, 1,3-diketones, and β-ketoesters, were selectively monofluorinated with...
The fluorination of 3-acetyl-2-oxindole with N-fluorobenzenesulfonimide under Lewis acid catalysis u...
fluorinated building blocks; fluoroarylacetic acid; fluoromalonate; fluorooxindole; organo-fluorine;...
An efficient difluorohydroxylation of substituted indoles leading to 3,3-difluoroindolin-2-ols with ...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
Fluorine chemistry plays a diverse role in the pharmaceutical, agricultural, and material industries...
Organofluorine compounds exhibit biological activity and have advantageous properties for drug desig...
Many pharmaceuticals have fused ring systems and their bioactivity tends to increase with the introd...
2015-07-17This dissertation mainly explored two aspects in organofluorine chemistry, the development...
A practical synthesis of α-fluorinated imides via the catalyst-free fluorohydroxylation of ynamides ...
3,3-Difluoro-2-oxindoles can be obtained directly from indoles in moderate yields <i>via</i> electro...
Organofluorine substrates are molecules of increasing demand in both academic and industrial setting...