Nucleotides, Part LXI , Phthaloyl Strategy: A New Concept of Oligonucleotide Synthesis
β Scribed by Markus Beier; Wolfgang Pfleiderer
- Publisher
- John Wiley and Sons
- Year
- 1999
- Tongue
- German
- Weight
- 177 KB
- Volume
- 82
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
With best personal wishes dedicated to Prof. Dr. Albert Eschenmoser on the occassion of his 75th birthday The syntheses of the 3'-O-(4,4'-dimethoxytrityl)-protected 5'-phosphoramidites 25 Β± 28 and 5'-(hydrogen succinates) 29 Β± 32, which can be used as monomeric building blocks for the inverse (5'-3'
Nucleotides. Part 54. Synthesis of Condensed N1-(2'-Deoxy-Ξ²-D-ribofuranosyl)lumazines, New Fluorescent Building Blocks in Oligonucleotide Synthesis. -Various condensed areno(g)lumazine derivatives (III) and (VI) are synthesized as new fluorescent aglycones for glycosylation reactions to form differe
Nucleotides. Part 55. Synthesis and Application of a Novel Linker for Solid-Phase Synthesis of Modified Oligonucleotides. -New linker molecules (I)-(IV) are prepared as alternatives to start oligonucleotide syntheses on solid supports. They have the potential to modify additionally the sugar moiety