In order to evaluate the effect of a new 2%-carbohydrate modification on the hybridization properties of oligonucleotides, uridine 2%-O-carbamates were synthesized and incorporated into DNA strands. The key intermediate in the synthesis, a mixed succinimide carbonate 2, was treated with various amin
Synthesis and structural and thermodynamic properties of oligonucleotides containing 2′-O-phosphorylated ribonucleosides
✍ Scribed by Hiroyuki Tsuruoka; Koh-ichiroh Shohda; Takeshi Wada; Mitsuo Sekine
- Book ID
- 104255747
- Publisher
- Elsevier Science
- Year
- 1996
- Tongue
- French
- Weight
- 273 KB
- Volume
- 37
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Conformation of the sugar, backbone and glycosidic bond of synthetic 2'-O-phosphorylated diuridylate U(2'-p)pU 1 was studied by NMR and CD. It was found that the 5' upstream ribose has predominantly an S-type of conformation. Tridecadeoxyuridylates incorporating a 2'-O-phosphorylated uridine U(2'-p) at the 3rd or 7th position were prepared by use of the polymer support synthesis and the effect of the 2'-O-phosphoryl group on the stability of the DNA duplex with dAi3 was examined. Both Tin experiments of these DNA duplexes and MD simulations of a duplex of dU3U(2'-p)dU3/dA7 suggested U(2'-p) has an extremely rigid S-type conformation when incorporaWal into the DNA duplex.
📜 SIMILAR VOLUMES
## Abstract Cyclohexyl nucleosides with an adenine and uracil base have been synthesized from 2‐azidocyclohexane‐1,5‐diol. The obtained racemic nucleosides were resolved using (__R__)‐__O__‐methylmandelic acid. Short oligonucleotides were synthesized using phorphoramidite chemistry. However, these
## 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 “Full Text” option. The original article is trackable v