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. 1976 Mar;3(3):709–720. doi: 10.1093/nar/3.3.709

The effective synthesis of uridylyl/3'-5'/5-methylcytidylyl/3'-5'/guanosine.

K Golankiewicz, A Jankowski
PMCID: PMC342935  PMID: 1272795

Abstract

The triester method was adapted to the synthesis of uridylyl/3'-5'/5-methylcytidylyl/3'-5'/guanosine. As the protecting groups 4-methoxy-5,6-dihydro-2H-pyran for 2'-OH and 5'-OH groups of uridine and 2'-OH group of 5-methylcytidine, methoxymethylidene for I:3'-cis-diol system of guanosine, and benzoyl for the amino groups of 5-methylcytidine and guanosine were used. The obtained product was characterised by UV, electrophoresis, chromatography, an enzymatic digestion and alkaline hydrolysis.

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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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