The use of a polymeric solid support loaded with a long alkyl chain quaternary ammonium allows the rapid and efficient recovery of cyclotron produced [18F]F- from [18O]water to a low water content organic solution compatible with fast nucleophilic labelling of most precursors for PET radiopharmaceuticals in high yield
Nucleophilic radiofluorination is an efficient synthetic route to many positron-emission tomography ...
International audienceAbstractIntroduction Since 1991 until now, many radiosyntheses of [18F]FLT hav...
The radioisotope 18F is often considered the best choice for PET imaging, owing to its desirable che...
The 18F labeling of radiopharmaceuticals requires nearly anhydrous solutions of [18F]fluoride. Aque...
Due to the short half-life of [18F] (half-life = 110min), the synthesis and purification ofradiotrac...
Efficient aliphatic radiofluorination in a mixed organic solvent system was investigated. This metho...
Improved methods for the production of ^{18}F have been developed. The isotope, a beta^{+} emitter w...
Positron emission tomography (PET) employs short half-life positron emitting isotopes, typically 18F...
The positron-emitting radionuclide fluorine-18 plays a prominent role in radiopharmaceuticals for po...
The unnatural isotope fluorine-18 (18F) is used as a positron emitter in molecular imaging. Currentl...
The design and construction of an automated synthesis system for radiopharmaceuticals labeled with 1...
For experiments with {sup 18}F beams the output of the SNICS ion source for fluorine ions was invest...
Fluoroform is an interesting motif for the isotopologue labelling of biologically active compounds w...
The expansion of [18F]-radiolabelling methodologies is vital for the advancement of Positron Emissio...
The availability of radiolabelled probes is important for in vivo studies by positron emission tomog...
Nucleophilic radiofluorination is an efficient synthetic route to many positron-emission tomography ...
International audienceAbstractIntroduction Since 1991 until now, many radiosyntheses of [18F]FLT hav...
The radioisotope 18F is often considered the best choice for PET imaging, owing to its desirable che...
The 18F labeling of radiopharmaceuticals requires nearly anhydrous solutions of [18F]fluoride. Aque...
Due to the short half-life of [18F] (half-life = 110min), the synthesis and purification ofradiotrac...
Efficient aliphatic radiofluorination in a mixed organic solvent system was investigated. This metho...
Improved methods for the production of ^{18}F have been developed. The isotope, a beta^{+} emitter w...
Positron emission tomography (PET) employs short half-life positron emitting isotopes, typically 18F...
The positron-emitting radionuclide fluorine-18 plays a prominent role in radiopharmaceuticals for po...
The unnatural isotope fluorine-18 (18F) is used as a positron emitter in molecular imaging. Currentl...
The design and construction of an automated synthesis system for radiopharmaceuticals labeled with 1...
For experiments with {sup 18}F beams the output of the SNICS ion source for fluorine ions was invest...
Fluoroform is an interesting motif for the isotopologue labelling of biologically active compounds w...
The expansion of [18F]-radiolabelling methodologies is vital for the advancement of Positron Emissio...
The availability of radiolabelled probes is important for in vivo studies by positron emission tomog...
Nucleophilic radiofluorination is an efficient synthetic route to many positron-emission tomography ...
International audienceAbstractIntroduction Since 1991 until now, many radiosyntheses of [18F]FLT hav...
The radioisotope 18F is often considered the best choice for PET imaging, owing to its desirable che...