The eeterificatlon of the hydroxyllc function in position8 2' or 3' of the terminal adenoslne unit of the soluble (tran8fer) ribonucleic acid by an emin acid repreeent8 an important step in the biosynth88is of proteins (1). Although no non-enzymatic method8 for the attechaent Of an miuOaCy1 residue
Synthesis of cytidyl(3'-5')adenosine bearing 2'(3')-O-leucyl ester via a phosphorothioate triester intermediate
β Scribed by Hitoshi Hotoda; Ryuichi Saito; Mitsuo Sekine; Tsujiaki Hata
- Book ID
- 104204127
- Publisher
- Elsevier Science
- Year
- 1990
- Tongue
- French
- Weight
- 733 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0040-4020
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β¦ Synopsis
2'(3')-0-(LeucylICpA was synthesized in the phosphotriester method . The phenylthio group was used as a protecting group of the Internucleotidlc bond. The P-S bond of the trlcster intermedlate was sclectlvely cleaved by using (BuaSnIZO under neutral conditions without cleavage of the leucyl ester bond.
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