Synthesis and properties of ApU analogs containing 2'-halo-2'-deoxyadenosines. Effects of 2' substituents on oligonucleotide conformation
β Scribed by Uesugi, Seiichi; Kaneyasu, Toshinori; Ikehara, Morio
- Book ID
- 126123553
- Publisher
- American Chemical Society
- Year
- 1982
- Tongue
- English
- Weight
- 946 KB
- Volume
- 21
- Category
- Article
- ISSN
- 0006-2960
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
Oligodeoxyribonucleotides containing 1 -deaza-2'-deoxyadenosine ( = 7-amino-3-(2-deoxy#? -D-erythro -pentofuranosyl)-3H-imidazo[4,5-b]pyridine; lb) form Hoogsteen duplexes. Warson-Crick base pairs cannot be built up due to the absence of N(1). For these studies, oligonucleotide building blocksthe ph
## Abstract Cyclohexyl nucleosides with an adenine and uracil base have been synthesized from 2βazidocyclohexaneβ1,5βdiol. The obtained racemic nucleosides were resolved using (__R__)β__O__βmethylmandelic acid. Short oligonucleotides were synthesized using phorphoramidite chemistry. However, these