N a t i o n a l Laboratory, Upton, NY 11973 Received Sumary A r a p i d , one-pot, s y n t h e s i s of cyclopropane [ llC]carbonyl c h l o r i d e was developed. This s y n t h e s i s proceeded i n 807; r a d i ochemical y i e l d (EOB) i n a s y n t h e s i s time of LO minutes. This a c i d c h
One-pot synthesis of [11C]ureas via triphenylphosphinimines
✍ Scribed by Erica W. van Tilburg; Albert D. Windhorst; Margreet van der Mey; Jacobus D. M. Herscheid
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- French
- Weight
- 148 KB
- Volume
- 49
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
A series of ^11^C‐labeled ureas was prepared using a rapid and efficient one‐pot procedure. First, the intermediate [^11^C]phenylisocyanate was formed with phenyltriphenylphosphinimine and [^11^C]CO~2~. A range of amines was then reacted with the [^11^C]phenylisocyanate yielding the [^11^C]urea derivatives in short synthesis times. This easy‐to‐handle method circumvents disadvantages of known procedures and generates the possibility to prepare other kinds of ^11^C‐labeled compounds using a variety of phenylphosphinimines in combination with different nucleophiles. The presented approach is an alternative to the use of established methods in ^11^C‐labeling chemistry. Copyright © 2006 John Wiley & Sons, Ltd.
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