Oligoribonucleotides, six to fifteen units long, were synthesized on a controlled pore glass support using ribonucleoside 3'-0-phosphoramidite reagents. Average coupling yieids of up to 98% were obtained with dirsopropylamrnophosphoramidite derivatives. In light of the increasing interest in the ro
Preparation of glyceronucleoside phosphoramidite synthons and their use in the solid phase synthesis of acyclic oligonucleotides
โ Scribed by Nassim Usman; Carl D. Juby; Kelvin K. Ogilvie
- Publisher
- Elsevier Science
- Year
- 1988
- Tongue
- French
- Weight
- 293 KB
- Volume
- 29
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
โฆ Synopsis
The syntheses of N,N-diisopropylmethylphosphoramidites (3a,b) of 9-I [Zdimethoxytrityl-hydroxy-l-(hydroxymethyl)ethoxy]-methyl)N6-benzoyladenine, 2a, and l-{ [Zdimethoxytritylhydroxy-1-(hydroxymethyl)ethoxy]-methyl)thymine, 2b, are described. Oligoacyclonucleotides, 2 -8 units long, were synthesized using these synthons on either controlled pore glass or silica gel
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