𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The synthesis of 123m Te-labeled 17β -hydroxy-2-tellura-A-nor-5α-androstane

✍ Scribed by F. F. Knapp Jr

Publisher
John Wiley and Sons
Year
1980
Tongue
French
Weight
451 KB
Volume
17
Category
Article
ISSN
0022-2135

No coin nor oath required. For personal study only.

✦ Synopsis

Abstract

A microscale synthesis has been developed for the preparation of 17β‐hydroxy‐2‐tellura‐A‐nor‐5α‐androstane. Reactorproduced ^123m^Te has been used to prepare the ^123m^Te labeled steroid. The radiochemical synthesis and purification of this potential prostate imaging agent are described in detail.

📜 SIMILAR VOLUMES

ChemInform Abstract: A Solution-Phase Co
ChemInform Abstract: A Solution-Phase Combinatorial Parallel Synthesis of 3β-Amido-3α-hydroxy-5α-androstane-17-ones.
✍ R. MALTAIS; D. POIRIER 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB 👁 1 views

A Solution-Phase Combinatorial Parallel Synthesis of 3β-Amido-3α-hydroxy-5α-androstane-17-ones. -A two-level library of title compounds (IV) is prepared via reaction of oxirane (I) with 4 primary amines followed by treatment of each set with 4 aliphatic acyl chlorides. The purities of the products

ChemInform Abstract: Synthesis of (25R)-
ChemInform Abstract: Synthesis of (25R)-17α-Hydroxy-22-oxocholest-5-ene-3β,16β,26-triyl Triacetate: A One-Pot Approach to the Protected Aglycon Analogue of OSW-1.
✍ Maria A. Fernandez-Herrera; Ma. G. Hernandez-Linares; Gabriel Guerrero-Luna; Soc 📂 Article 📅 2011 🏛 John Wiley and Sons ⚖ 28 KB 👁 1 views

## Abstract The spirostanic side chain of pennogenin (I) can be quantitatively transformed under mild acidic conditions in a 22‐oxocholestanic framework through a one‐step procedure.