The synthesis of two backbone modified dinucleotide analogues is described in which the natural phosphodiester linkage is replaced by a 3'-5" c~xbazoyl linkage. In both cases the bridge was formed through a coupling reaction between an appropriate 3'-carbazoyl nucleoside analogue and an aldehyde nuc
Synthesis of sulfamide linked dinucleotide analogues
β Scribed by Jason Micklefield; Kevin J. Fettes
- Publisher
- Elsevier Science
- Year
- 1997
- Tongue
- French
- Weight
- 220 KB
- Volume
- 38
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
β¦ Synopsis
Novel sulfamide [-NHSO2NH-] linked dinucleotide analogues d(TnsnT) and d(TnsnA) have been synthesised from 3"--and 5"-amino nucleosides. Treatment of these amino nucleosides with catechol sulfate results in the formation of 2-hydroxyphenyl sulfamate esters which couple smoothly in good yields with either 5"--or 3"-amines of similar nucleosides. NMR studies showed that the 3"sulfamide group results in a preferential C3"--endo (Northern) sugar conformation.
π SIMILAR VOLUMES
Protected formacetal-linked purine-purine dinucleotide analogs, including dG-f-dG, dG-f-dA, dA-f-dG, and dA-f-dA, were synthesized for the first time in 40 -60% yields by condensation of the 5'-OH group with the 3'-OCH2SCH3 group of the two corresponding deoxynucleoside units using N-iodosuccinimide
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a βFull Textβ option. The original article is trackable v