UNNATURAL NUCLEOSIDES AND NUCLEOTIDES. III.
Direct preparation of 14C-labeled 5-allyl- and 5-propyl-2′-deoxyuridine from [2- 14C]2′-deoxyuridine
✍ Scribed by Jerry L. Ruth; Steven K. White; Donald E. Bergstrom
- Publisher
- John Wiley and Sons
- Year
- 1982
- Tongue
- French
- Weight
- 246 KB
- Volume
- 19
- Category
- Article
- ISSN
- 0022-2135
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✦ Synopsis
Abstract
[2‐^14^C]5‐Allyl‐2′‐deoxyuridine was synthesized directly from [2‐^14^C]2′‐deoxyuridine using mercury, palladium, and 3‐chloropropene. [2‐^14^C]5‐Propyl‐2′‐deoxyuridine was obtained by hydrogenation of the [^14^C]5‐allyl‐2′‐deoxy‐uridine. Advantages of the synthetic method and its application to the preparation of other radiolabeled 5‐alkyl/alkeny1‐2′‐deoxyuridines are discussed.
📜 SIMILAR VOLUMES
therefore been incorporated in this isoprenoid. The
## Abstract A convenient method for preparing 5__H__‐2,3‐benzodi‐azepines labelled with ^14^C was developed in which the corresponding phenylacetone derivatives were acylated by labelled aromatic carboxylic acid. In spite of the low yield, this method is advantageous in comparison the known ones be