𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The synthesis of 2′–5′ linked oligoribonucleotides

✍ Scribed by Kelvin K. Ogilvie; Nicole Y. Theriault


Publisher
Elsevier Science
Year
1979
Tongue
French
Weight
212 KB
Volume
20
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.

✦ Synopsis


The use of alkylsilyl protecting groups provides a rapid route to 3',5'diprotected ribonucleosides which are easily coupled via the phosphorodichloridite procedure to produce 2'-5' linked ribonucleotides.

It has recently been demonstrated l-3 that 2'-5' linked oligoadenylic


📜 SIMILAR VOLUMES


A convenient synthesis of 2−–5− linked o
✍ Y. Hayakawa; M. Uchiyama; T. Nobori; R. Noyori 📂 Article 📅 1985 🏛 Elsevier Science 🌐 French ⚖ 245 KB

A general synthesis of 2'-5' linked oligoribonucleotides has been achieved on the basis of chemoselective formation of the 2'-5' internucleotide linkage using N-unblocked nucleosides. The 2'-5' linked oligoadenylates (2-5As) produced from ATP in the

Nonenzymatic Ligation of Short-Chained 2
✍ Hiroaki Sawai; Makoto Wada; Tsukasa Kouda; Akiko Nakamura Ozaki 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 133 KB

## Abstract 5′‐pACUG tetraribonucleotides containing 2′–5′ or 3′–5′ linkages self‐condensed on 2′–5′‐ or 3′–5′‐linked complementary decaribonucleotide (5′‐CAGUCAGUCA) templates. CD and UV melting studies showed that helix formation took place in all four possible combinations of linkage isomers of

Incompatibility of acid-labile 2′ and 5′
✍ Chris Christodoulou; Sudhir Agrawal; Michael J. Gait 📂 Article 📅 1986 🏛 Elsevier Science 🌐 French ⚖ 152 KB

Cleavage of 2'-0-tetrahydropyranyl groups from ribonucleoside derivatives used in solid-phase oligoribonucleotide synthesis takes place to an unacceptable extent during treatment with protic acid to remove 5'-O-pixyl groups.