The blood f l o w reagent 4-iodoantipyrine, l a b e l l e d w i t h 13'1 o r lZ5I, was prepared by a l l o w i n g aqueous a n t i p y r i n e t o r e a c t w i t h e i t h e r no-carrier-added 1311o r lZ5I-i n t h e presence o f c h l orami ne-T. P u r i f i c a t i o n o f 4-[ 13'I]i odoanti p y r
No-carrier-added bromination of estrogens with chloramine-t and Na77Br
✍ Scribed by J. K. Mazaitis; B. E. Francis; W. C. Eckelman; R. E. Gibson; R. C. Reba; J. W. Barnes; G. E. Bentley; P. M. Grant; H. A. O'Brien Jr
- Publisher
- John Wiley and Sons
- Year
- 1981
- Tongue
- French
- Weight
- 230 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The syntheses of monobromohexestrol and 17α‐bromoethynylestradiol are described as examples of bromination of phenolic and ethynyl moieties using Chloramine‐T. This technique represents a unique method of producing no‐carrier‐added radiobromoethynylderivatives. However, more efficient chromatography is needed to separate the chloroderivative, which is a side product of the reaction, from the radio‐bromoderivative.
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