Solid phase glycosidation of oligonucleotides
β Scribed by Matteo Adinolfi; Gaspare Barone; Lorenzo De Napoli; Luigi Guariniello; Alfonso Iadonisi; Gennaro Piccialli
- Book ID
- 104261023
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- French
- Weight
- 216 KB
- Volume
- 40
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
CPG-bound nucleosides (deoxyguanosine excepted) can be stereoselectively glycosylated in high yield at their 5'-hydroxyl by a "disarmed" trichioroacetimidate donor in the presence of stoichiometric amounts of TMSOTf (5 eq.) and in short reaction times. These results allowed the solid-phase synthesis of an oligonucleotide functionalized at both ends with sugar residues.
π SIMILAR VOLUMES
A general procedure for the synthesis of branched RNA and DNA oligonucleotides has been developed. The synthetic strategy involves the 3'->5' synthesis of a DNA or RNA oligomer on a solid-phase, controlled-pore glass support with an automated DNA synthesizer. The branch point nucleoside is introduce