S e c t i o n o f R a d i o l o g y a n d N u c l e a r M e d i c i n e and Department o f C h e m i s t r y , H a m i l t o n , O n t a r i o , Canada, L8N 325 SUHMARY R e a c t i o n o f d i l u t e [ F -l 8 ] f l u o r i n e gas w i t h e i t h e r m e l g t o n i n o r 5 -h y d r o x y -t r y p
Synthesis of [18F]fluoro-labeled progestins for PET
โ Scribed by Tjibbe J. De Groot; Aalt Verhagen; Philip H. Elsinga; Willem Vaalburg
- Book ID
- 103922605
- Publisher
- Elsevier Science
- Year
- 1991
- Weight
- 407 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0883-2889
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โฆ Synopsis
The synthesis of 21-[18F]fluoro-16 alpha-methyl-19-norprogesterone, 21-[18F]fluoro-16 alpha-ethyl-19-norprogesterone, 21-[18F]fluoro-16 alpha-methylprogesterone and 21-[18F]fluoro-16 alpha-ethylprogesterone is described. These compounds are prepared with a specific activity greater than 200 TBq/mmol (5000 Ci/mmol) from the corresponding tosylates in 10% radiochemical yield (EOB). A remote controlled system has been developed for this synthesis.
๐ SIMILAR VOLUMES
The synthesis of a pyrimidine analog, 3 0 -deoxy-3 0 -[ 18 F]-fluoro-1-b-d-xylofuranosyluracil ([ 18 F]-FMXU) is reported. 5-Methyluridine 1 was converted to its dimethoxytrityl derivatives 2 and 3 as a mixture. After separation the 2 0 , 5 0 -di-methoxytrityluridine 2 was converted to its 3 0 -trif