Oxidative Fluorination with 18F Fluoride New Radiochemistry for PET Imaging
"The objective of this proposal is to provide a solution to a well-recognised problem in 18F-radiochemistry: the direct fluorination of electron rich aromatics with a nucleophilic source of 18F-Fluoride. The value of this new radi...
ver más
¿Tienes un proyecto y buscas un partner? Gracias a nuestro motor inteligente podemos recomendarte los mejores socios y ponerte en contacto con ellos. Te lo explicamos en este video
Proyectos interesantes
SELEFLU
Synthesis and Evaluation of 18F Labelled N F Reagents
201K€
Cerrado
Fecha límite de participación
Sin fecha límite de participación.
Descripción del proyecto
"The objective of this proposal is to provide a solution to a well-recognised problem in 18F-radiochemistry: the direct fluorination of electron rich aromatics with a nucleophilic source of 18F-Fluoride. The value of this new radiochemistry will be challenged with the synthesis of 6-[18F]Fluoro-L-3,4-dihydroxyphenylalanine ([18F]FDOPA) and 6-[18F]Fluoro-L-meta-tyrosine ([18F]FMT), two high value tracers to image the presynaptic sites of the dopaminergic system; yet these two radiotracers are notoriously difficult to produce using currently available radiochemistry. Conceptually, we advance that the nucleophilic fluorination of electron rich aromatics with fluoride may be possible using a so-called substrate umpolung approach. Under oxidative condition, we will revert the reactivity profile of the substrate from a nucleophilic to an electrophilic entity (umpolung), thereby allowing for nucleophilic 18F-labelling. This approach, which will rely heavily on microfluidic technology, has never been exploited for 18F-radiolabelling."