Reactions of difluorocarbene with benzyl and alkylzinc halides leading to fluorinated organozinc species have been described. The generated α-difluorinated organozinc reagents are reasonably stable in solution and can be quenched with external electrophiles (iodine, bromine, proton), affording compounds containing the CF<sub>2</sub> fragment
The first direct and straightforward nucleophilic fluoromethylation of organic compounds is reported...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
1,1-Difluoro-1-alkenes bearing a biaryl-2-yl group effectively underwent site-selective intramolecul...
A method for the coupling of organozinc reagents, difluorocarbene, and allylic electrophiles is desc...
(1,1,2,2-Tetrafluorobut-3-en-1-yl)zinc bromide was prepared by insertion of the zinc–silver couple i...
The trifluoromethylation of carbonyl compounds is accomplished by the stable (trifluoromethyl)zinc r...
In view of the expanding interest in fluorinated heterocycles, the installation of a fluoroalkyl gro...
Mechanism of olefin difluorocarbenation catalyzed by hypervalent organobismuth complex, discovered r...
Fluorobenzenes, in particular fluorobenzene (FB) and 1,2-difluorobenzene (1,2-DiFB), are increasingl...
Fluorobenzenes, in particular fluorobenzene (FB) and 1,2-difluorobenzene (1,2-DiFB), are increasingl...
The dissertation work that is summarized in this thesis describes novel syntheses of organofluorine ...
After a general introduction about the properties and preparation of organofluorine compounds (Chapt...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
The first direct and straightforward nucleophilic fluoromethylation of organic compounds is reported...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
1,1-Difluoro-1-alkenes bearing a biaryl-2-yl group effectively underwent site-selective intramolecul...
A method for the coupling of organozinc reagents, difluorocarbene, and allylic electrophiles is desc...
(1,1,2,2-Tetrafluorobut-3-en-1-yl)zinc bromide was prepared by insertion of the zinc–silver couple i...
The trifluoromethylation of carbonyl compounds is accomplished by the stable (trifluoromethyl)zinc r...
In view of the expanding interest in fluorinated heterocycles, the installation of a fluoroalkyl gro...
Mechanism of olefin difluorocarbenation catalyzed by hypervalent organobismuth complex, discovered r...
Fluorobenzenes, in particular fluorobenzene (FB) and 1,2-difluorobenzene (1,2-DiFB), are increasingl...
Fluorobenzenes, in particular fluorobenzene (FB) and 1,2-difluorobenzene (1,2-DiFB), are increasingl...
The dissertation work that is summarized in this thesis describes novel syntheses of organofluorine ...
After a general introduction about the properties and preparation of organofluorine compounds (Chapt...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
The development of organofluorine chemistry has revolutionised the way many agrochemical and pharmac...
The first direct and straightforward nucleophilic fluoromethylation of organic compounds is reported...
This thesis concerns method development of new synthetic routes by applying electrophilic hypervalen...
1,1-Difluoro-1-alkenes bearing a biaryl-2-yl group effectively underwent site-selective intramolecul...