The gem-difluoroethylene moiety is considered as a valuable building block in organic synthesis, but methods to introduce it into small molecules are generally limited to specific substrates. Here, the authors demonstrate that a gem-difluorovinyl iodonium salt enables the direct difluoroethylation reactions of a diverse range of N- and O-nucleophiles
2015-07-20This dissertation is divided into two parts. The first part describes the generation of th...
A hypervalent iodine reagent-based α-carbonyl dihalogenation reaction is reported. Treating diazoace...
Fluorination is an important strategy for perturbing the biophysical properties of compounds in medi...
Organic compounds containing a gem-difluoromethylene group are useful for a variety of applications ...
The incorporation of the gem-difluoromethylene (CF2) group into organic frameworks is highly sought ...
Background: 1,1-Difluoroalkenes cannot only be used as valuable precursors for organic synthesis, bu...
We report an optimised and highly efficient synthetic route towards a valuable functionalised fluori...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Molecular scaffolds containing alkylfluorine substituents are desired in many areas of chemical rese...
We report the transition-metal-free defluorinative C-C bond-forming reaction of trifluoromethyl alke...
UnrestrictedThis dissertation describes the development of new methodologies for nucleophilic monofl...
Reported herein is the application of fluoroallylboration for the synthesis of gem-difluorinated com...
Organofluorine substrates are molecules of increasing demand in both academic and industrial setting...
Hypervalent iodine compounds have been established as useful reagents in synthetic chemistry due to ...
2,2-Diaryl-1,3-dithiolanes, readily obtainable from diaryl ketones, were transformed into the corres...
2015-07-20This dissertation is divided into two parts. The first part describes the generation of th...
A hypervalent iodine reagent-based α-carbonyl dihalogenation reaction is reported. Treating diazoace...
Fluorination is an important strategy for perturbing the biophysical properties of compounds in medi...
Organic compounds containing a gem-difluoromethylene group are useful for a variety of applications ...
The incorporation of the gem-difluoromethylene (CF2) group into organic frameworks is highly sought ...
Background: 1,1-Difluoroalkenes cannot only be used as valuable precursors for organic synthesis, bu...
We report an optimised and highly efficient synthetic route towards a valuable functionalised fluori...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
Molecular scaffolds containing alkylfluorine substituents are desired in many areas of chemical rese...
We report the transition-metal-free defluorinative C-C bond-forming reaction of trifluoromethyl alke...
UnrestrictedThis dissertation describes the development of new methodologies for nucleophilic monofl...
Reported herein is the application of fluoroallylboration for the synthesis of gem-difluorinated com...
Organofluorine substrates are molecules of increasing demand in both academic and industrial setting...
Hypervalent iodine compounds have been established as useful reagents in synthetic chemistry due to ...
2,2-Diaryl-1,3-dithiolanes, readily obtainable from diaryl ketones, were transformed into the corres...
2015-07-20This dissertation is divided into two parts. The first part describes the generation of th...
A hypervalent iodine reagent-based α-carbonyl dihalogenation reaction is reported. Treating diazoace...
Fluorination is an important strategy for perturbing the biophysical properties of compounds in medi...