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. 1987 May 11;15(9):3761–3772. doi: 10.1093/nar/15.9.3761

A new solid-phase synthesis of oligoribonucleotides by the phosphoro-p-anisidate method using tetrahydrofuranyl protection of 2'-hydroxyl groups.

S Iwai, E Yamada, M Asaka, Y Hayase, H Inoue, E Ohtsuka
PMCID: PMC340780  PMID: 3588309

Abstract

Six nonaribonucleotides containing the 5'-splice site, one complementary nonamer and an octadecamer containing the 3'-splice site have been synthesized on a polymer support using the phosphoro-p-anisidate method. A 5'-linked 2'-O-tetrahydrofuranyl-N-protected nucleoside 3'-(o-chlorophenyl)phosphoro-p-anisidate was used as the starting nucleotide, and the chain elongated in the 3'-direction by removing the p-anisidate protecting group with isoamyl nitrite under neutral conditions. The octadecamer has been synthesized using dinucleotide blocks and a 3'-terminal trinucleotide.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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