𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Preparation of 16α-[18F]fluoroestradiol-3-sulphamate and 16α-[18F]fluoroestradiol-17β-sulphamate in an automated module

✍ Scribed by J. Römer; F. Füchtner; J. Steinbach; H. Kasch

Book ID
112132785
Publisher
John Wiley and Sons
Year
2001
Tongue
French
Weight
124 KB
Volume
44
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Simultaneous preparation of 16α-[18F]flu
Simultaneous preparation of 16α-[18F]fluoroestradiol-sulphamates in an automated module. A high-yield procedure for 16α-[18F]fluoroestradiol-17β-sulphamate
✍ J. Römer; F. Füchtner; J. Steinbach; H. Kasch 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 French ⚖ 119 KB

## Abstract After successfully synthesizing 16__α__‐[^18^F]fluoroestradiol‐3,17__β__‐disulphamate in an automatic procedure, we studied the conditions for obtaining 16__α__‐[^18^F]fluoroestradiol‐monosulphamates in a similar manner. The described procedure can simultaneously provide approximately 3

NCA 16α-[18F]fluoroestradiol-17β: The ef
NCA 16α-[18F]fluoroestradiol-17β: The effect of reaction vessel on fluorine-18 resolubilization, product yield, and effective specific activity
✍ James W. Brodack; Michael R. Kilbourn; Michael J. Welch; John A. Katzenellenboge 📂 Article 📅 1986 🏛 Elsevier Science ⚖ 500 KB

Although the reported synthesis of the title compound resulted in a high radiochemical yield (43% based on resolubilized 18F), the effective specific activity at EOS was low (166 Ci/mmol). Reduction in the amount of carrier fluoride in the target water improved the effective specific activity of the