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The synthesis of some tritiated 5-substituted uracil derivatives
✍ Scribed by P. J. Barr; A. S. Jones; R. T. Walker; L. Bohá
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- French
- Weight
- 273 KB
- Volume
- 16
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
The synthesis of 5‐[^3^H‐ethynyl]uracil and 5‐acetyl[6‐^3^H]uracil in good yield and of a medium specific activity ( > 40 mCi/mmol) is described. The compounds are necessary for following the incorporation of these and other derived 5‐substituted uracils into DNA and also for studying the metabolism and mode of action of their deoxynucleosides, some of which possess antiviral properties.
📜 SIMILAR VOLUMES
## Abstract Thiation of **1** by LR gave the corresponding 3,5‐dithioxo derivative **2** and the trimer **3**. Methylation of **1** afforded the S‐methyl derivative **4**. Compound **1** was fused with 6‐bromo‐2‐phenyl‐benzo[1,3‐d]oxazin‐4‐one **(****5****)** and gave **6**. Condensation of **1** w