Preparation of high specific activity tr
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D. Zhong; Anita H. Lewin
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Article
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2009
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John Wiley and Sons
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French
⚖ 289 KB
## Abstract Fluocinolone acetonide was tritiated by selective reduction of the 1,2‐double bond of the __O__‐protected analog under tritium, followed by re‐establishment of the 1,2‐double bond and deprotection. Protection of both hydroxyl functionalities was required. The product was obtained with s