Synthesis of pppA2′p5′A2′p5′A γ-amidates by one pot procedure from A2′p5′A2′p5′A
✍ Scribed by Ágnes Nyilas
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 269 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
One pot synthesis of prnidate of pppA2'p5'A2'p5'A described here using phosphoroxychloride and bis-tri-n-butylammonium pyrophosphate for preparing cyclic trimetaphosphate intermediate opening up with n-decylamin. 01997 Elsevier ScienceLtd.
The 5'-phosphorylation of 2',5'A analogues helps them to bind to endoribonuclease', but a phosphataae degrades it. Therefore it is important to synthesize phosphatase resistant analoguesz. Altough
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