## Abstract Oligonucleotides containing terminal phosphate groups serve as useful intermediates for different applications in molecular and cell biology, as well as for diagnostic purposes. The chemical synthesis of these derivatives has been an important topic of oligonucleotide research. We repor
A novel solid support for synthesis of 2′,3′-cyclic phosphate terminated oligonucleotides
✍ Scribed by Joseph S Vyle; Nicholas H Williams; Jane A Grasby
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- French
- Weight
- 293 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Michaelis-Arbusov chemistry was used to prepare O,S-dialkyl Y-O-nucleosidyl phosphorothiolate triesters in solution and attached to CPG.
The support-bound nucleoside was utilised in the synthesis of a pentaribonucleotide that was fully deprotected on the support. Subsequent ~'eatment with a buffered solution of iodine cleaved the RNA l~om the CPG with concomitant formation of a terminal 2',Y-cyclic phosphate.
📜 SIMILAR VOLUMES
The novel 2',3'-cyclic phosphate (1) derived from 2'-homouridine has been prepared by phosphorylation with 2-cyanoethyl N,N~V',N"-tetraisopropylphosphorodiamidite.
A novel solid phase synthesis of 3'-phosphorylated oligonuclcotides is described. The chain assembly is carried out by phosphoramidite strategy on solid support 2, which allows a mild and fast release of the oligonueleotide in solution. The applicability of the method is demonstrated by preparation