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Synthesis of a Novel, Optically Active Uridine Analog Containing a 1,4-Dioxane Sugar Moiety. Synthesis of the Corresponding Dinucleotide.
- Source :
-
Nucleosides, Nucleotides & Nucleic Acids . Mar2009, Vol. 28 Issue 3, p220-237. 18p. 15 Diagrams. - Publication Year :
- 2009
-
Abstract
- A new optically active uridine nucleoside analogue in which a substituted 1,4-dioxane ring functioned as the sugar analogue was prepared from L-tartaric acid. The nucleoside analogue was further converted into the corresponding protected dinucleotide. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NUCLEOSIDES
*DIOXANE
*TARTARIC acid
*SUGARS
*ENANTIOMERS
Subjects
Details
- Language :
- English
- ISSN :
- 15257770
- Volume :
- 28
- Issue :
- 3
- Database :
- Academic Search Index
- Journal :
- Nucleosides, Nucleotides & Nucleic Acids
- Publication Type :
- Academic Journal
- Accession number :
- 37223050
- Full Text :
- https://doi.org/10.1080/15257770902865407