| Literature DB >> 4088863 |
H Inoue, Y Hayase, M Asaka, A Imura, S Iwai, K Miura, E Ohtsuka.
Abstract
2'-O-Methyl derivatives of common ribonucleosides were prepared from appropriately protected nucleosides via the methylation of the 2'-hydroxyl groups with methyl iodide or diazomethane. These derivatives were converted into 2'-O-methylribonucleotide units and the guanosine derivative was linked to a polymer support. Thus, oligo(2'-O-methylribonucleotides) having the sequence of AmCmUmUmAmCmCmUmGm was synthesized in a stepwise manner by using the phosphotriester method. Thermal stabilities (Tm's) of the hybrid between the 2'-O-methyl ribooligomer and the complementary ribooligomer and of the related hybrids are compared. The synthesis of ribooligomer by a new approach is also described.Entities:
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Year: 1985 PMID: 4088863
Source DB: PubMed Journal: Nucleic Acids Symp Ser ISSN: 0261-3166