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Novel Synthetic Approach to Multibenzoylated Nucleosides.
- Source :
-
Synthetic Communications . 2008, Vol. 38 Issue 9, p1346-1354. 9p. 2 Diagrams, 1 Chart. - Publication Year :
- 2008
-
Abstract
- An improved and highly efficient synthetic approach to multibenzoylated nucleosides bearing free 5'-hydroxyl groups is described here. By employing t-butyldimethylsilyl (TBDMS) rather than the more commonly used dimethoxytrityl (DMTr) as a temporary 5'-OH protecting group of the starting nucleoside, this methodology provides the expected products in nearly quantitative yields, thereby substantially reducing the cost and effort of synthesis. [ABSTRACT FROM AUTHOR]
- Subjects :
- *NUCLEOSIDES
*NUCLEOTIDES
*HYDROXYL group
*RADICALS (Chemistry)
*ORGANIC synthesis
Subjects
Details
- Language :
- English
- ISSN :
- 00397911
- Volume :
- 38
- Issue :
- 9
- Database :
- Academic Search Index
- Journal :
- Synthetic Communications
- Publication Type :
- Academic Journal
- Accession number :
- 31632299
- Full Text :
- https://doi.org/10.1080/00397910801916280