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.

Automation of [11C]acyl chloride syntheses using commercially available 11C-modules

Matarrese M;
2002

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.
2002
Istituto di Bioimmagini e Fisiologia Molecolare - IBFM
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/163057
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