http://www.cnr.it/ontology/cnr/individuo/prodotto/ID10023
Automation of [11C]acyl chloride syntheses using commercially available 11C-modules (Articolo in rivista)
- Type
- Label
- Automation of [11C]acyl chloride syntheses using commercially available 11C-modules (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Matarrese M., Sudati F., Soloviev D., Todde S., Turolla E.A., Galli Kienle M., Fazio F. (2002)
Automation of [11C]acyl chloride syntheses using commercially available 11C-modules
in Applied radiation and isotopes
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Matarrese M., Sudati F., Soloviev D., Todde S., Turolla E.A., Galli Kienle M., Fazio F. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Note
- ISI Web of Science (WOS) (literal)
- Titolo
- Automation of [11C]acyl chloride syntheses using commercially available 11C-modules (literal)
- Abstract
- In implementing published procedures for the incorporation of [11C]carbon
dioxide on the immobilized Grignard reagents for the radiosynthesis
[11C]acyl chlorides, several modifications of a Nuclear Interface PET
Tracer Synthesizer Module for 11C-methylations were made to obtain reliable
and reproducible production processes for routine clinical applications.
High yields of [carbonyl-11C]WAY-100635 and [11C]zofenoprilat were obtained
via 11C-carboxylation using [carbonyl-11C]cyclohexanecarbonyl chloride and
2-methyl-[1-11C]acryloyl chloride prepared with the modified module. (literal)
- Prodotto di
- Autore CNR
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